Eu Ivdr Eu Ivd Class B On The Market

IDS Androstenedione

Devices (same UDI-DI)
3
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
05060169691261
Basic UDI-DI Code
5060169691261WY
Reference
IS-5400
Device Types
None provided
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market

Additional Description

IDS Androstenedione assay is an automated in vitro diagnostic device intended for the quantitative determination of androstenedione in human serum on the IDS system. Results are to be used in conjunction with other clinical and laboratory data as an aid in the diagnosis of androgen disorders in adult and pediatric populations.

CND Nomenclature Codes

Code Description
W0102050101 ANDROSTENEDIONE

Available In Countries

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇾 Cyprus 🇨🇿 Czechia 🇩🇪 Germany 🇩🇰 Denmark 🇪🇪 Estonia 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇭🇷 Croatia 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇸 Iceland 🇮🇹 Italy 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden 🇸🇮 Slovenia 🇸🇰 Slovakia 🇹🇷 Türkiye 🇬🇧 United Kingdom

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