Standards Worldwide
Standards Worldwide
Phone +49 30 58885700-07

Draft technical rule [WITHDRAWN]

VDI 5701:2016-09 - Draft

Biomaterials in medicine - classification,requirements and applications

German title
Biomaterialien in der Medizin - Klassifikation, Anforderungen und Anwendungen
Publication date
2016-09
Original language
German
Pages
36

from 106.60 EUR VAT included

from 99.63 EUR VAT excluded

Format and language options

PDF download 1
  • 106.60 EUR

Shipment (3-5 working days) 1
  • 118.60 EUR

Monitor with the Standards Ticker

1

 Attention: Document withdrawn!

Easily subscribe: Save time and money now!

You can also subscribe to this document - together with other important standards in your industry. This makes your work easier and pays for itself after a short time.

Sparschwein_data
Subscription advantages
Sparschwein Vorteil 1_data

Important standards for your industry, regularly updated

Sparschwein Vorteil 2_data

Much cheaper than buying individually

Sparschwein Vorteil 3_data

Useful functions: Filters, version comparison and more

Publication date
2016-09
Original language
German
Pages
36

Quick delivery via download or delivery service

Buy securely with a credit card or pay upon receipt of invoice

All transactions are encrypted

Short description
Use and application of biomaterials in the medical field are subject of this standard. Additionally to the definition of biomaterials and adjacent terms in the fields of material sciences, biology, and medicine, the scopes of application are presented on the living organism. The standard delimits materials for the application on humans and animals, and elaborates determining properties of a biomaterial. In the standard, requirements for the qualification of materials as biomaterials are determined which are based on the actual use and are able to ensure the detection of relevant properties, particularly biocompatibility. The standard is addressed to scientists, developers, manufacturers and processors of biomaterials for medical devices as well as their users. It supports the fulfilment of regulatory requirements for marketing of medical devices.
Content
ICS
11.040.01, 11.100.20
Replacement amendments

This document has been replaced by: VDI 5701:2018-05 .

Also available in
Loading recommended items...
Loading recommended items...
Loading recommended items...
Loading recommended items...