Eu Ivdr Eu Ivd Class B On The Market

Human Comp ELISA

Devices (same UDI-DI)
1
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
05060169696662
Basic UDI-DI Code
5060169696662YR
Reference
AC-23F1
Device Types
None provided
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market

Additional Description

Human COMP ELISA is an in vitro diagnostic device intended for the quantitative determination of Cartilage Oligomeric Matrix Protein (COMP) in human serum. Results are to be used in conjunction with other clinical and laboratory data as an aid in the prognosis and monitoring of cartilage degradation in conditions such as rheumatoid arthritis and osteoarthritis.

CND Nomenclature Codes

Code Description
W0102060399 BONE METABOLISM TESTS - OTHER

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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