Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
MYCOPLASMA ANTIBODY ASSAYS
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.
Free to try · every answer cites its records
Basic Information
- Primary DI
- 06975132463013
- Basic UDI-DI Code
- B-06975132463013
- Reference
- IMC-402G-20
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Jiangsu Accuracy Biotechnology Co.,Ltd.
Additional Description
This product is used for in vitro qualitative detection of Mycoplasma pneumoniae and Chlamydia pneumoniae IgM antibodies in human serum or whole blood.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105010802 | MYCOPLASMA ANTIBODY ASSAYS |
| W0105010116 | CHLAMYDIA PNEUMONIAE ANTIBODY IGM |
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