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BioCLIA Autoimmune Reagent Kit, gp210
EUDAMEDClass IVD General (EU MDR)
Ref MY00114CModel gp210, 50 Tests/KitRef MY00165Model gp210, 100 Tests/Kit
Identity
- Trade Name
- BioCLIA Autoimmune Reagent Kit, gp210 EUDAMED
- Device Name
- BioCLIA Autoimmune Reagent Kit, gp210 EUDAMED
- Model / Reference
- gp210, 50 Tests/Kit EUDAMEDMY00114C EUDAMEDgp210, 100 Tests/Kit EUDAMEDMY00165 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06924030415631 EUDAMED06924030402808 EUDAMED
- Basic UDI-DI
- B-06924030415631 EUDAMEDB-06924030402808 EUDAMED
- EMDN Code
- W0102100799 AUTOIMMUNE HEPATITIS - OTHER EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
Yes
EUDAMEDEUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
BioCLIA Autoimmune Reagent Kit, gp210 by HOB Biotech Group Corp., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-06924030415631 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- HOB Biotech Group Corp., Ltd.
- EUDAMED SRN
- CN-MF-000023974
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED bdfdc67e-7c14-4249-931b-351be315d552 61 fields · synced Jul 11, 2026
- EUDAMED 1359b777-1b55-4a0e-9d5c-b1a0011818a9 61 fields · synced May 19, 2026