Eu Ivdd
Eu Ivd General
On The Market
🇹🇷 Türkiye
RapidFor™ hsCRP / CRP Rapid Test Kit (FIA)
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 08683548250193
- Basic UDI-DI Code
- B-08683548250193
- Reference
- VMPO11
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Vitrosens Biyoteknoloji Anonim Şirketi
Additional Description
This test is suitable for in vitro quantitative detection of the concentration of C-reactive protein in human serum, plasma, and whole blood. This product is provided for testing by medical and health institutions and is used for auxiliary diagnosis of patients' inflammation and other related diseases.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W01021308 | HIGH-SENSITIVITY C-.REACTIVE PROTEIN |
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).
BluBox
Device
EU IVDD
·
Eu Ivd General
·Blusense Diagnostics ApS·On the market·5 countries
extendSURE™ HbA1c Liquid Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·19 countries
ViroTrack Sero COVID-19 Total Ab
Device
EU IVDD
·
Eu Ivd General
·Blusense Diagnostics ApS·On the market·5 countries
extendSURETM Haemoglobin F and A2 Calibrators
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·8 countries
extendSURE™ Haemoglobin F and A2 Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·8 countries
extendSURE™ HbA1c Liquid Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·19 countries