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Chlamydia Rapid Test Device (Swab/Urine)
EUDAMEDClass IVD Annex II List B (EU MDR)
Ref ICH-502
Identity
- Device Name
- Chlamydia Rapid Test Device (Swab/Urine) EUDAMED
- Model / Reference
- ICH-502 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-ICH-502MW EUDAMED
- Basic UDI-DI
- B-ICH-502MW EUDAMED
- EMDN Code
- W0105090101 CHLAMYDIA AG - RT & POC EUDAMED
Classification
- Device Class
- Class IVD Annex II List B EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
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
Chlamydia Rapid Test Device (Swab/Urine) by Abon Biopharm(Hangzhou) Co., Ltd — Class IVD Annex II List B — IVDD — listed in EUDAMED
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-ICH-502MW | Class IVD Annex II List B | Active |
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Manufacturer
- Manufacturer
- Abon Biopharm(Hangzhou) Co., Ltd
- EUDAMED SRN
- CN-MF-000009171
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (1)
- EUDAMED 57cfb181-ac2e-4fa5-9912-b04dc1fc8b3f 61 fields · synced Oct 6, 2026