Identity
- Trade Name
- GLUCO TEST Lanzetten 1 St. EUDAMED
- Device Name
- Blood Sterile Lancet EUDAMED
- Model / Reference
- TD-5084 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04251575910409 EUDAMED
- Basic UDI-DI
- B-04251575910409 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 1 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-04251575910409 | 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 a870ee90-387b-4acb-9444-1204f7b0e0b8 61 fields · synced Jun 17, 2026