GPDR
Privatumo politika
projektai-lsd Lietuvos standartizacijos departamentas
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Projekto etapai

1. Prioritetinių darbo temų pažymėjimas ir ekspertų skyrimas
2. Projektas
3. Viešoji apklausa
Nuo 2025-12-07 iki 2026-02-05
4. Closure of enquiry
5. Submission to Formal Vote

Organizacija

CEN Europos standartizacijos komitetas

Technikos komitetas

TK 32 Sveikata

Užsienio technikos komitetas

CEN/TC 205

Komentarų skaičius

0

Komentavimo pradžia

2025-12-07

Taikymo sritis

ISO 7886-1:2017 specifies requirements and test methods for verifying the design of empty sterile single-use hypodermic syringes, with or without needle, made of plastic or other materials and intended for the aspiration and injection of fluids after filling by the end-users. This document does not provide requirements for lot release. The syringes are primarily for use in humans. Sterile syringes specified in this document are intended for use immediately after filling and are not intended to contain the medicament for extended periods of time. It excludes syringes for use with insulin (see ISO 8537), single-use syringes made of glass, syringes for use with power-driven syringe pumps, syringes pre-filled by the manufacturer, and syringes intended to be stored after filling (e.g. in a kit for filling by a pharmacist). Hypodermic syringes without a needle specified in this document are intended for use with hypodermic needles specified in ISO 7864.

Ryšiai

Pakeis
LST EN ISO 7886-1:2018