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LH Assay kit CLIA
EUDAMEDClass IVD General (EU MDR)
Ref SUPM060072Ref SUPM060036
Identity
- Trade Name
- LH Assay kit CLIA EUDAMED
- Device Name
- LH Assay kit CLIA EUDAMED
- Model / Reference
- SUPM060072 EUDAMEDSUPM060036 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06974521004233 EUDAMED06974521004226 EUDAMED
- Basic UDI-DI
- B-06974521004233 EUDAMEDB-06974521004226 EUDAMED
- EMDN Code
- W0102050105 LUTEINISING HORMONE EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Ireland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
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
LH Assay kit CLIA by Shenzhen Superbio Technology Co., 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-06974521004233 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Shenzhen Superbio Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000024149
- Authorised Representative
- QbD RepS BV BE-AR-000000040
Sources (2)
- EUDAMED 008c7539-96ea-4180-94b2-6f145f624364 61 fields · synced Jul 25, 2026
- EUDAMED d215dfd9-1be0-4d1f-bf25-a03718653ff3 61 fields · synced May 18, 2026