Eu Ivdr
Eu Ivd Class B
On The Market
🇧🇪 Belgium
Vedolizumab ELISA
Devices (same UDI-DI)
1
Certificates
0
Countries
4
Notified Bodies
0
Basic Information
- Primary DI
- 05430000412070
- Basic UDI-DI Code
- 5430000412710501Q2
- Reference
- 710501
- Device Types
-
Single use
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class B
- Status
- On The Market
- Manufacturer
- Advanced Practical Diagnostics
Additional Description
The Vedolizumab ELISA is an in vitro diagnostic medical device for professional laboratory use, intended to quantitatively measure vedolizumab in serum or plasma samples. The kit is designed for manual use and for use on open ELISA automates. Measurement of vedolizumab is intended to be performed for monitoring the drug level in the context of therapeutic drug monitoring in patients undergoing therapy with vedolizumab.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102080799 | AUTOIMMUNE DISEASE TDM - OTHER |
Available In Countries
🇧🇪 Belgium
🇱🇺 Luxembourg
🇳🇱 Netherlands
🇸🇮 Slovenia
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