Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
M.Pneumonia IgG/IgM Rapid Test Device(whole blood/serum/plasma)
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06976753472866
- Basic UDI-DI Code
- B-06976753472866
- Reference
- A120501D
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Hangzhou Cybereagen Biotech Co., Ltd.
Additional Description
M.Pneumonia IgG/IgM Rapid Test Device (whole blood, serum or plasma) is for the qualitative detection of IgG and IgM antibodies to Mycoplasma pneumoniae in whole blood, serum or plasma as an aid in the diagnosis of Mycoplasma pneumoniae infection.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105010802 | MYCOPLASMA ANTIBODY ASSAYS |
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