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Basic Information
- Primary DI
- 05404035100264
- Basic UDI-DI Code
- 54040351221020BU
- Reference
- 221020
- Device Types
-
Single use
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class B
- Status
- On The Market
- Manufacturer
- Cypress Diagnostics
Additional Description
The Cypress Diagnostics kit CRP Latex is an in vitro diagnostic medical device intended to be used for the qualitative detection of C-Reactive Protein (CRP) in human serum. The device is not automated. The detection of CRP is intended to be used for the detection of systemic inflammatory processes due to an active disease. This kit is intended to be used by healthcare professionals in a laboratory-based testing environment. For in vitro diagnostic use only. For professional use only.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W01021109 | C-REACTIVE PROTEIN |
Available In Countries
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd Class B) and regulation (EU IVDR).