Healthcare
Safety and quality are non-negotiable in the medical devices industry.
Regulatory requirements for medical devices are increasingly stringent throughout every step of a product’s life cycle, including service and delivery.
The International Organization for Standardization (ISO) is an independent organization dedicated to publishing quality and risk management standards for product development in a variety of industries, including medical devices.
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Standards Library
Access the latest European Voluntary Standards. All documents are officially verified and regularly updated to reflect current regulations.
18
Standards
5
Categories
PDF
+ DOCX
Type
Name
Language
Format
Healthcare, ISO
ISO 7199-2024 Vs ISO 7199-2017
Cardiovascular implants and artificial organs — Blood-gas exchangers (oxygenators)
English
$55.00
including VAT
$35.00
including VAT
$95.00
including VAT
ISO
ISO 2002-001 2026 Versus ISO 2002-001 2005
Financial services — Universal financial industry message scheme
Part 1: Metamodel
English
$55.00
including VAT
$35.00
including VAT
$75.00
including VAT
Healthcare, ISO
EN ISO 1135-5_2025 vs EN ISO 1135-5_2015
Transfusion sets for single use with pressure infusion apparatus
English
$75.00
including VAT
$35.00
including VAT
$110.00
including VAT
ISO, Software
ISO 29100:2024 VERSUS ISO 29100:2020
Information technology — Security techniques — Privacy framework.
English
$30.00
including VAT
$30.00
including VAT
$55.00
including VAT