Identity
- Trade Name
- GLUCO TEST Lanzetten 10 St. EUDAMED
- Device Name
- Sterile Blood Lancet EUDAMED
- Model / Reference
- TD-5084 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04251575910294 EUDAMED
- Basic UDI-DI
- B-04251575910294 EUDAMED
- EMDN Code
- V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
GLUCO TEST Lanzetten 10 St. by Taidoc Technology Corporation — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04251575910294 | Class IIa | Active |
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Manufacturer
- Manufacturer
- TaiDoc Technology Corporation
- EUDAMED SRN
- TW-MF-000017956
- Authorised Representative
- MedNet EC-REP GmbH DE-AR-000000002
Sources (1)
- EUDAMED 49dfd050-09e9-4702-a50a-1657ff32c85e 61 fields · synced Jun 19, 2026