Eu Ivdr Eu Ivd Class B On The Market 🇧🇪 Belgium

Adalimumab ELISA

Advanced Practical Diagnostics · 🇧🇪 Belgium
Devices (same UDI-DI)
1
Certificates
0
Countries
4
Notified Bodies
0

Basic Information

Primary DI
05430000412056
Basic UDI-DI Code
5430000412710201PK
Reference
710201
Device Types
Single use
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market

Additional Description

The Adalimumab ELISA is an in vitro diagnostic medical device intended to be used by healthcare professionals for the quantitative measurement of adalimumab in serum or plasma samples. The kit is designed for manual use and for use on open ELISA automates. Measurement of adalimumab is intended to be performed for monitoring the drug level in the context of therapeutic drug monitoring in patients undergoing therapy with adalimumab.

CND Nomenclature Codes

Code Description
W0102080702 ADALIMUMAB

Available In Countries

🇧🇪 Belgium 🇱🇺 Luxembourg 🇳🇱 Netherlands 🇸🇮 Slovenia

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