EN ISO 14708-4:2022
Current
The latest, up-to-date edition.
Implants for surgery - Active implantable medical devices - Part 4: Implantable infusion pump systems (ISO 14708-4:2022)
27-07-2022
This document specifies particular requirements for active implantable medical devices intended to deliver a medicinal substance to site-specific locations within the human body, to provide basic assurance of safety for both patients and users. It amends and supplements ISO14708-1:2014. The requirements of this document take priority over those of ISO14708-1.This document is applicable to active implantable medical devices intended to deliver medicinal substances to site-specific locations within the human body.This document is also applicable to some non-implantable parts and accessories of the devices defined in Clause3.The tests that are specified in this document are type tests intended to be carried out on a sample of a device to show compliance and are not intended to be used for the routine testing of manufactured products.NOTE This document is not intended to apply to non-implantable infusion systems.
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| NF EN ISO 14708-4:2022 | Identical |
| DS/EN ISO 14708-4:2022 | Identical |
| UNI EN ISO 14708-4 : 2022 | Identical |
| ÖVE/ÖNORM EN ISO 14708-4:2023 01 15 | Identical |
| PN-EN ISO 14708-4:2023-01 | Identical |
| VDE 0750-20-4:2023-09 | Identical |
| DIN EN ISO 14708-4:2023-09 | Identical |
| UNE-EN ISO 14708-4:2023 | Identical |
| SN EN ISO 14708-4:2022 | Identical |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.