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prSSH EN ISO 20417:2025

Informacion i dhënë nga prodhuesi me pajisje mjekësore

Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12)

General information

10.00     3 dhj 2025

DPS

DPS/KT 6

European Norm

11.040.01  

Scope

NOTE 1        There is guidance or rationale for this Clause contained in Clause A.2.
This document specifies the requirements for information supplied by the manufacturer for a medical device or by the manufacturer for an accessory, as defined in 3.1. This document includes the generally applicable requirements for identification and labels on a medical device or accessory, the packaging, marking of a medical device or accessory, and accompanying information. This document does not specify the means by which the information is to be supplied.
NOTE 2        Some authorities having jurisdiction impose different requirements for the identification, marking and documentation of a medical device or accessory.
Specific requirements of medical device product standards or group standards take precedence over requirements of this document.

Life cycle

PREVIOUSLY

WITHDRAWN
SSH EN 1041:2008+A1:2013

WITHDRAWN
SSH EN 1041:2008

NOW

IN_DEVELOPMENT
prSSH EN ISO 20417:2025
10.00 Proposal for new project registered
3 dhj 2025

Related project

Adopted from EN ISO 20417:2021 IDENTICAL

Adopted from ISO 20417:2021 IDENTICAL