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prEN 843-9 Viešoji apklausa
Komentavimo iki data 2026-07-30
Modernioji techninė keramika. Monolitinės keramikos mechaninės savybės kambario temperatūroje. 9 dalis. Bandymo metodas nustatyti atsparumą kraštų atsilupimui

This document specifies two test methods for the determination of the resistance of the edges of brittle ceramic materials to be damaged by chipping. This document is applicable to homogeneous monolithic ceramics with flat surfaces and straight sharp or chamfered edges.

prEN 14492-1 Viešoji apklausa
Komentavimo iki data 2026-07-30
Kranai. Varikliniai suktuvai ir keltuvai. 1 dalis. Varikliniai suktuvai

This document is applicable to the design, information for use, maintenance and testing of power-driven winches for which the prime mover is an electric motor, hydraulic motor, or pneumatic motor. Winches are designed for the movement or manipulation of loads supported on level or inclined planes in situations where risks resulting from a failure of the winding mechanism or pulling medium are mitigated by external measures. This document is not applicable to devices which handle suspended loads. Generally, a winch is used without any additional transport movement, except in cases where a winch is used on a stranded vehicle for self-recovery of the vehicle. Applications of winches covered are for example, but not limited to: a) rope winches; b) belt winches, except steel belts used as pulling media; c) traction winches, including double capstan and traction sheave winches. These types of winches a) to c) also include the following specific applications: — vehicle recovery winches; — winches for boat trailers; — winches for stationary offshore applications. NOTE Examples are shown in Annex H. This document does not apply to: — power-driven hoists in accordance with EN 14492-2; — forestry winches in accordance with EN ISO 19472-1; — winches for seagoing vessels and mobile offshore units; — winches for the lifting of persons; — NGL building hoists in accordance with EN 14492-2; — winches for the handling of hot molten masses. This document deals with the significant hazards, hazardous situations or hazardous events relevant to power driven winches when used as intended and under conditions of misuse which are reasonably foreseeable, identified in Annex A. This document does not specify additional requirements for hazards related to the use of power driven winches in explosive atmospheres in underground mines.

prEN ISO 10704 Viešoji apklausa
Komentavimo iki data 2026-07-12
Vandens kokybė. Visuminis alfa ir visuminis beta aktyvumas. Tyrimo metodas naudojant ploną šaltinio sluoksnį (ISO/DIS 10704:2025)

Warning — Persons using this document should be familiar with normal laboratory practice. This document does not purport to address all of the safety problems, if any, associated with its use. It is the responsibility of the user to establish appropriate safety and health practices. IMPORTANT — It is absolutely essential that tests conducted in accordance with this document be carried out by suitably qualified staff. This document specifies a method for the determination of gross alpha and gross beta activity concentrations for alpha- and beta-emitting radionuclides. Gross alpha and gross beta activity measurement is not intended to give an absolute determination of the activity concentration of all alpha and beta emitting radionuclides in a test sample, but is a screening analysis to ensure particular reference levels of specific alpha and beta emitters have not been exceeded. This type of determination is also known as gross alpha and gross beta index. Gross alpha and gross beta analysis is not expected to be as accurate nor as precise as specific radionuclide analysis after radiochemical separations. Maximum beta energies of approximately 0,1 MeV or higher are well measured. It is possible that low energy beta emitters cannot be detected (e.g. 3H, 55Fe, 241Pu) or can only be partially detected (e.g. 14C, 35S, 63Ni, 210Pb, 228Ra). If the presence of low-energy beta emitters is strongly suspected, liquid scintillation analysis is recommended (ISO 11704). The method described in this document applies to non-volatile radionuclides, since some gaseous or volatile radionuclides (e.g. radon and radioiodine) can be lost during the source preparation. The method described in this document is applicable to test samples of drinking water, rainwater, sea water, surface and ground water as well as cooling water, industrial water, domestic and industrial wastewater after proper sampling, sample handling and test sample preparation (filtration when necessary and taking into account the amount of dissolved material in the water). The method described in this document can be used in the event of an emergency situation, because the results can be obtained in less than 1 h. Detection limits reached for gross alpha and gross beta are less than 10 Bq·l-1 and 20 Bq·l-1, respectively, for instance for rainwater water. The evaporation of a 10 ml sample can be carried out in 20 min followed by 10 min counting using a gas-flow -proportional counter with window. It is the laboratory’s responsibility to ensure the suitability of this test method for the water samples tested.

prEN ISO 1924-2 Viešoji apklausa
Komentavimo iki data 2026-07-30
Popierius ir kartonas. Savybių nustatymas tempiant. 2 dalis. Pailgėjimo tempiant pastoviu greičiu metodas (20 mm/min) (ISO/DIS 1924-2:2026)

ISO 1924-2:2008 specifies a method for measuring the tensile strength, strain at break and tensile energy absorption of paper and board, using a testing machine operating at a constant rate of elongation (20 mm/min). ISO 1924-2:2008 also specifies equations for calculating the tensile index, the tensile energy absorption index and the modulus of elasticity. Testing in conformance with ISO 1924-2:2008 always includes the measurement of tensile strength. Measurement or calculation of other properties is subject to agreement between the parties concerned. ISO 1924-2:2008 is applicable to all papers and boards, including papers with a high strain at break if the results are within the capacity of the testing machine. It also applies to the components of corrugated board but not, however, to corrugated board itself.

prEN ISO 7198 Viešoji apklausa
Komentavimo iki data 2026-07-30
Širdies ir kraujagyslių implantai bei ekstrakorporinės sistemos. Kraujagyslių protezai. Vamzdiniai kraujagyslių transplantantai ir kraujagyslių lopai (ISO/DIS 7198:2026)

ISO 7198:2016 specifies requirements for the evaluation of vascular prostheses and requirements with respect to nomenclature, design attributes and information supplied by the manufacturer, based upon current medical knowledge. Guidance for the development of in vitro test methods is included in an informative annex to ISO 7198:2016. It can be considered as a supplement to ISO 14630:2012, which specifies general requirements for the performance of non-active surgical implants. NOTE Due to the variations in the design of implants covered by ISO 7198 :2016 and, in some cases, due to the relatively recent development of some of these implants (e.g. bioabsorbable vascular prostheses, cell based tissue engineered vascular prostheses), acceptable standardized in vitro tests and clinical results are not always available. As further scientific and clinical data become available, appropriate revision of ISO 7198 :2016 will be necessary. It is applicable to sterile tubular vascular grafts implanted by direct visualization surgical techniques as opposed to fluoroscopic or other non-direct imaging (e.g. computerized tomography or magnetic resonance imaging), intended to replace, bypass, or form shunts between segments of the vascular system in humans and vascular patches intended for repair and reconstruction of the vascular system. Vascular prostheses that are made of synthetic textile materials and synthetic non-textile materials are within the scope of ISO 7198:2016. While vascular prostheses that are made wholly or partly of materials of non-viable biological origin, including tissue engineered vascular prostheses are within the scope, ISO 7198:2016 does not address sourcing, harvesting, manufacturing and all testing requirements for biological materials. It is further noted that different regulatory requirements might exist for tissues from human and animal sources. Compound, coated, composite, and externally reinforced vascular prostheses are within the scope of ISO 7198:2016. Endovascular prostheses implanted using catheter delivery and non-direct visualization are excluded from the scope of ISO 7198:2016. It includes information on the development of appropriate test methods for graft materials, referenced in ISO 25539‑1 for materials used in the construction of endovascular prostheses (i.e. stent-grafts). NOTE Requirements for endovascular prostheses are specified in ISO 25539‑1. The valve component of valved conduits constructed with a tubular vascular graft component, and the combination of the valved component and the tubular vascular graft component, are excluded from the scope of ISO 7198:2016. It can be helpful in identifying the appropriate evaluation of the tubular vascular graft component of a valved conduit but specific requirements and testing are not described for these devices. Cardiac and pericardial patches, vascular stents, accessory devices such as anastomotic devices, staplers, tunnelers and sutures, and pledgets are excluded from the scope of ISO 7198:2016. NOTE Requirements for vascular stents are specified in ISO 25539‑2. Requirements regarding cell seeding are excluded from the scope of ISO 7198:2016. Tissue engineered vascular prostheses that contain or are manufactured using cells present many distinct manufacturing (e.g. aseptic processing, cell seeding, etc.) and testing issues than those produced with synthetic or non-viable biological materials. The in vitro testing requirements that are outlined in ISO 7198:201

prEN 1865-1 Viešoji apklausa
Komentavimo iki data 2026-07-30
Pacientų perkėlimo įranga, naudojama greitosios medicinos pagalbos automobiliuose. 1 dalis. Bendrosios neštuvų sistemos ir pacientų perkėlimo įranga

This document specifies minimum requirements for the design and performance of stretchers and other patient handling equipment used in road ambulances for the handling and carrying of patients. It aims to ensure patient safety and minimize the physical effort required by staff operating the equipment.

prEN 1865-3 Viešoji apklausa
Komentavimo iki data 2026-07-30
Pacientų perkėlimo įranga, naudojama greitosios medicinos pagalbos automobiliuose. 3 dalis. Tvirtieji neštuvai

This document specifies minimum requirements for the design and performance of heavy duty stretchers used in road ambulances for the treatment and transportation of patients. It aims to ensure patient safety and minimize the physical effort required by staff operating the equipment.

prEN 1865-4 Viešoji apklausa
Komentavimo iki data 2026-07-30
Pacientų perkėlimo įranga, naudojama greitosios medicinos pagalbos automobiliuose. 4 dalis. Sulankstoma paciento pernešimo kėdė

This document specifies minimum requirements for the design and performance of foldable patient transfer chairs, which are used for the conveyance of patients to and/or from road ambulances. It aims to ensure patient safety and to minimize the physical effort required by staff operating the equipment.

prEN ISO 7039 Viešoji apklausa
Komentavimo iki data 2026-07-28
Metalinės medžiagos. Tempimo bandymai. Medžiagų jautrumo aukšto slėgio dujų poveikiui tuščiaviduriuose bandiniuose įvertinimo metodas (ISO/DIS 7039:2026)

This document specifies the geometries and proposed finishing procedures of the inner surface of hollow test piece of metallic materials, filled with a high-pressure gaseous medium. The document specifies a tensile testing procedure to evaluate the effect of high-pressure gaseous medium compared to a high-pressure inert gas or air. The document can be used for the screening of metallic materials by evaluating mechanical property changes due to the effects of various test gases, including hydrogen. NOTE          Temperature range and pressure range depend on the materials to be tested and test gas to be used.

prEN 13142 Viešoji apklausa
Komentavimo iki data 2026-07-28
Pastatų vėdinimas. Gyvenamųjų pastatų vėdinimui skirti komponentai ir gaminiai. Reikalaujamosios ir pasirenkamosios eksploatacinės charakteristikos

This document specifies and classifies the component/product performance characteristics, which may be necessary for the design, rating and dimensioning, placing on the market of residential ventilation products and systems to provide the predetermined performance, comfort conditions of temperature, air velocity, humidity, hygiene and sound in the occupied zone. It defines those performance characteristics (mandatory or optional) which are determined, measured and presented according to relevant test methods. It provides a classification scheme, which leads to a full definition of product properties based on test methods described in various European Standards, and gives an overview of the test standards. Distinction between mandatory and optional requirements is left to each European and national regulation(s). The codification part in Annex B and the classification part in Clause 8 apply to the following products: - unidirectional mechanical supply and exhaust residential ventilation units according to EN 13141-4:2021 and EN 13141-6:2014; - ducted mechanical bidirectional residential ventilation units according to EN 13141-7:2021; - non-ducted mechanical bidirectional residential ventilation units according to EN 13141-8:2022. This document does not apply to other products such as filters, fire dampers, ducts, control devices and sound attenuators, which may also be incorporated in residential ventilation. This document specifies in Annex ZA and Annex ZB the requirements of EU 1253/2014 and EU 1254/2014 for residential ventilation units below 1 000 m3/h air volume flow. This document does not cover requirements raised by European Directives (e.g. low voltage directive, EMC directive) and other requirements such as corrosion, reaction to fire and snow penetration.

prEN 40000-10 Viešoji apklausa
Komentavimo iki data 2026-07-28
Esminiai produktų kibernetinio saugumo reikalavimai. 10 dalis. Produktai su skaitmeniniais elementais, naudojami tapatybės duomenų valdymo sistemose ir programinėje bei aparatinėje įrangoje, įskaitant tapatumo nustatymo ir prieigos kontrolės skaitytuvus, taip pat ir biometrinius skaitytuvus

This project aims at covering the line 16 of the standardisation request and will provide: • General description of the Product with digital elements belonging to that category and the product and/or components such Product with digital elements may integrate, including – amongst other: o detailed description of that product category using in:  Identity management systems hardware and software are products with digital elements that provide mechanisms for identity lifecycle management, such as identity provisioning, maintenance, authentication, authorisation and deprovisioning, and including associated metadata.  Privileged access management hardware and software are products with digital elements that authenticate and authorise users or devices, granting or denying access to digital resources or to physical locations.  This category includes but is not limited to products (hardware, software and communication protocol) with digital elements that have the core functionality of either or both identity management and privileged access management; authentication and access control readers; biometric readers; single sign-on software; federated identity management software, protection and safety management (such as access control, intrusion alarm, CCTV and fire safety systems) and multi-factor authentication software. o Intended product purpose and reasonably foreseeable use in the above categories; o Identification of the various types of Products with digital elements; o Delineation and interplay with the following other categories of Product with digital elements (identified by their line in the standardization request):  line 17  line 18  line 20  line 24  line 28  line 29  line 32  line 35  line 37  line 38  line 39  line 41 • Description of their life cycle; • Relevance of cybersecurity essential requirements including the cybersecurity assessment requirements; • Definition of applicable risk profiles to be considered for these Product with digital elements; • Applicable cybersecurity requirements ensuring fulfillment of the essential requirements for each risk profile; • Applicable cybersecurity assessment requirements for each risk profile. A base document is provided • Defining the risk profiles; • Identifying initial cybersecurity security requirements.

prEN 40000-11 Viešoji apklausa
Komentavimo iki data 2026-07-28
Esminiai produktų kibernetinio saugumo reikalavimai. 11 dalis. Fizinį gaubtą turinti aparatinė įranga su apsauginiu korpusu, suprojektuota saugumo funkcijoms, tokioms kaip saugus duomenų saugojimas ir kriptografinės operacijos atviroje aplinkoje, atlikti

This document defines cyber security requirements for products with digital elements belonging to product category “Hardware Device with Security Boxes” (hereinafter called “Product” or “HWSB product”). The technical description of “Hardware Devices with Security Boxes” can be found in Annex II of [CRA]. The Hardware Devices with Security Boxes in scope are designed for deployment in a range of environments and where the threat landscape includes attackers with various attack potential. HWSB are hardware-based systems intended to provide secure storage, processing and use of sensitive data, including cryptographic assets, within a protected hardware boundary (envelope). This document applies to the HWSB part of the product. The applicability of this document to specific products is determined based on their intended purpose, use case and risk assessment.

prEN ISO 3630-7 Viešoji apklausa
Komentavimo iki data 2026-07-28
Odontologija. Endodontiniai instrumentai. 7 dalis. Ultragarsiniai instrumentų antgaliai (ISO/DIS 3630-7:2026)

This document is applicable to endodontic ultrasonic inserts, operated in combination with either air or electrically powered stand-alone handpieces or handpieces connecting to dental units. This document specifies requirements and test methods for inserts, and requirements for marking, labeling and packaging.

prEN 13201-3 Viešoji apklausa
Komentavimo iki data 2026-07-28
Kelių apšvietimas. 3 dalis. Eksploatacinių charakteristikų skaičiavimas

This European Standard specifies the conventions and mathematical procedures to be adopted in calculating the photometric performance of road lighting installations designed in accordance with the parameters described in EN 13201-2 to ensure that every lighting calculation is based on the same mathematical principles. The design procedure of a lighting installation also requires the knowledge of the parameters involved in the described model, their tolerances and variability. These aspects are not considered in this part of EN 13201 but a procedure to analyse their contribution in the expected results is suggested in EN 13201-4 and it can also be used in the design phase.

prEN ISO/IEC 19788-3 Viešoji apklausa
Komentavimo iki data 2026-07-28
Informacinės technologijos mokymuisi, ugdymui ir rengimui. Mokymosi išteklių metaduomenys. 3 dalis. Pagrindinis taikomųjų programų profilis (ISO/DIS 19788-3:2026)

The primary purpose of ISO/IEC 19788 is to specify metadata elements and their attributes for the description of learning resources. This includes the rules governing the identification of data elements and the specification of their attributes. ISO/IEC 19788 provides data elements for the description of learning resources and resources directly related to learning resources. ISO/IEC 19788-3:2011 is designed to help implementers with a starting point for adopting ISO/IEC 19788, defining an application profile that specifies, through adding constraints to the use of some data elements, how the ISO/IEC 19788-2 element set can be used.

prEN ISO 25237 Viešoji apklausa
Komentavimo iki data 2026-07-28
Sveikatos informatika. Pseudonimų suteikimas (ISO/DIS 25237:2026)

ISO 25237:2017 contains principles and requirements for privacy protection using pseudonymization services for the protection of personal health information. This document is applicable to organizations who wish to undertake pseudonymization processes for themselves or to organizations who make a claim of trustworthiness for operations engaged in pseudonymization services. ISO 25237:2017 - defines one basic concept for pseudonymization (see Clause 5), - defines one basic methodology for pseudonymization services including organizational, as well as technical aspects (see Clause 6), - specifies a policy framework and minimal requirements for controlled re-identification (see Clause 7), - gives an overview of different use cases for pseudonymization that can be both reversible and irreversible (see Annex A), - gives a guide to risk assessment for re-identification (see Annex B), - provides an example of a system that uses de-identification (see Annex C), - provides informative requirements to an interoperability to pseudonymization services (see Annex D), and - specifies a policy framework and minimal requirements for trustworthy practices for the operations of a pseudonymization service (see Annex E).

prEN ISO 14111 Viešoji apklausa
Komentavimo iki data 2026-07-28
Gamtinės dujos. Metrologinės sieties gairės (ISO/DIS 14111:2026)
prEN ISO 21606 Viešoji apklausa
Komentavimo iki data 2026-07-23
Odontologija. Pagalbiniai elastomeriniai ortodontijos reikmenys (ISO/DIS 21606:2026)

This document specifies the requirements and their test methods applicable to all elastomeric auxiliaries used for orthodontics both inside and outside the mouth, in conjunction with fixed and removable appliances.

prEN 820-5 Viešoji apklausa
Komentavimo iki data 2026-07-23
Modernioji techninė keramika. Monolitinės keramikos termomechaninės savybės. 5 dalis. Tampros modulių nustatymas aukštoje temperatūroje

This part of EN 820 describes methods for determining the elastic moduli, specifically Young's modulus, shear modulus and Poisson's ratio, of advanced monolithic technical ceramics at temperatures above room temperature. The standard prescribes three alternative methods for determining some or all of these three parameters: A the determination of Young's modulus by static flexure of a thin beam in three- or four-point bending. B the determination of Young's modulus by forced longitudinal resonance, or Young's modulus, shear modulus and Poisson's ratio by forced flexural and torsional resonance, of a thin beam. C the determination of Young's modulus from the fundamental natural frequency of a struck bar (impulse excitation method). This part of EN 820 extends the above-defined room-temperature methods described in EN 843-2 to elevated temperatures. All the test methods assume the use of homogeneous test pieces of linear elastic materials. The test assumes that the test piece has isotropic elastic properties. At high porosity levels all of the methods can become inappropriate. The maximum grain size (see EN 623-3), excluding deliberately added whiskers, should be less than 10 % of the minimum dimension of the test piece. NOTE 1 Method C in EN 843-2 based on ultrasonic time of flight measurement has not been incorporated into this part of EN 820. Although the method is feasible to apply, it is specialised, and outside the capabilities of most laboratories. There are also severe restrictions on test piece geometries and methods of achieving pulse transmission. For these reasons this method has not been included in EN 820-5. NOTE 2 The upper temperature limit for this test depends on the properties of the test pieces, and can be limited by softening within the timescale of the test. In addition, for method A there can be limits defined by the choice of test jig construction materials.

prEN 843-2 Viešoji apklausa
Komentavimo iki data 2026-07-23
Modernioji techninė keramika. Monolitinės keramikos mechaninės savybės kambario temperatūroje. 2 dalis. Jungo modulio, šlyties modulio ir Puasono koeficiento nustatymas

This part of EN 843 specifies methods for determining the elastic moduli, specifically Young’s modulus, shear modulus and Poisson’s ratio, of advanced monolithic technical ceramics at room temperature. This European Standard prescribes four alternative methods for determining some or all of these three parameters: A The determination of Young’s modulus by static flexure of a thin beam in three- or four-point flexure. B The determination of Young’s modulus by forced longitudinal resonance, or Young’s modulus, shear modulus and Poisson’s ratio by forced flexural and torsional resonance, of a thin beam. C The determination of Young’s modulus, shear modulus and Poisson’s ratio from the time-of-flight of an ultrasonic pulse. D The determination of Young’s modulus from the fundamental natural frequency of a struck bar (impulse excitation method). All the test methods assume the use of homogeneous test pieces of linear elastic materials. NOTE 1 Not all ceramic materials are equally and linearly elastic in tension and compression, such as some porous materials and some piezoelectric materials. With the exception of Method C, the test assumes that the test piece has isotropic elastic properties. Method C may be used to determine the degree of anisotropy by testing in different orientations. NOTE 2 An ultrasonic method for dealing with anisotropic materials (ceramic matrix composites) can be found in ENV 14186 (see Bibliography). An alternative to Method D for isotropic materials using disc test pieces is given in Annex A. NOTE 3 At high porosity levels all of the methods except Method C can become inappropriate. The methods are only suitable for a maximum grain size (see EN 623-3), excluding deliberately added whiskers, of less than 10 % of the minimum dimension of the test piece. NOTE 4 The different methods given in this European Standard can produce slightly different results on the same material owing to differences between quasi-isothermal quasi-static an

prEN 13201-2 Viešoji apklausa
Komentavimo iki data 2026-07-23
Kelių apšvietimas. 2 dalis. Eksploatacinių charakteristikų reikalavimai

This part of this European Standard defines performance requirements which are specified as lighting classes for road lighting aiming at the visual needs of road users, and it considers environmental aspects of road lighting. NOTE Installed luminous intensity classes for the restriction of disability glare and control of obtrusive light and installed glare index classes for the restriction of discomfort glare are defined in the informative Annex A. Lighting of pedestrian crossings is discussed in the informative Annex B. Disability glare evaluation for conflict areas (C classes) and pedestrian and pedal cyclists (P classes) is discussed in the informative Annex C.

prEN ISO 14880-1 Viešoji apklausa
Komentavimo iki data 2026-07-23
Optics and photonics - Microlens arrays - Part 1: Vocabulary (ISO/DIS 14880-1:2026)

This document defines terms for microlens arrays. It applies to arrays of very small lenses formed inside or on one or more surfaces of a common substrate. This document also applies to systems of microlens arrays.

prEN 13914-1 Viešoji apklausa
Komentavimo iki data 2026-07-23
Išorės ir vidaus tinko projektavimas, paruošimas ir dengimas. 1 dalis. Išorės tinkas

This document specifies requirements and recommendations for the design, preparation and application of - renders based on cement, lime or other mineral binders, and/or combinations thereof, masonry cement and polymer modified binder based external renderings, in accordance with EN 998-1 or site made renders; - renders based on organic binders in accordance with EN 15824 on all common types of backgrounds. It includes rendering on both new and old backgrounds and the maintenance and repair of existing work. This document gives guidance on the use of established site, factory and semi-finished factory-made renders. This document does not cover the following: a) the use and application of special renders for liquid retaining structures, e.g. coatings, and for backgrounds to cladding systems; b) the structural repair of concrete; c) the installation of external thermal insulation composite systems (ETICS); d) the specification and use of sealants used to seal joints for use with rendering; e) the use of gypsum-based renders; f) renders on historical monuments or buildings in protected areas; g) the design and installation of flashings at windowsills and elsewhere. Because of the many varied materials, practices and different climatic conditions, it is not possible for certain aspects of the standard to enter into sufficient detail to be fully usable by all practitioners. NOTE Local or national regulations take precedence when applicable.

prEN 13914-2 Viešoji apklausa
Komentavimo iki data 2026-07-23
Išorės ir vidaus tinko projektavimas, paruošimas ir dengimas. 2 dalis. Vidaus tinkas

This document deals with the design considerations and essential principles for internal plastering systems and application of plastering systems. The different parts of the EN 13914 series of standards specify requirements and recommendations for detailing, design and material considerations, the selection of mixes and the application of gypsum plasters, gypsum/lime plasters, lightweight plasters, lime/gypsum-, cement- and cement/lime-based plasters, lime-based plasters, clay plasters, silicate plasters, organic plasters, polymer-modified plasters, etc. This document does not deal with the following: - external finishes; - painting and/or preparation; - impregnations; - structural repair of concrete; - prefabricated fibre-reinforced plaster elements; - surface treatments. Because of the many varied materials, practices and different climatic conditions, it is not possible for certain aspects of the standard to enter into sufficient detail to be fully usable by all practitioners. NOTE Local or national regulations take precedence when applicable.

prEN ISO 10993-11 Viešoji apklausa
Komentavimo iki data 2026-07-23
Biologinis medicinos priemonių įvertinimas. 11 dalis. Sisteminio toksiškumo tyrimai (ISO 10993-11:2025)

ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.

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