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Gluceofine Pro Blutentnahme-Lanzetten

EUDAMED

Class IIa (EU MDR)

Ref TD-5084

by TaiDoc Technology Corporation

Identity

Trade Name
Gluceofine Pro Blutentnahme-Lanzetten EUDAMED
Device Name
Sterile Lancets EUDAMED
Model / Reference
TD-5084 EUDAMED

Identifiers

Primary DI / UDI-DI
04260315240096 EUDAMED
Basic UDI-DI
47104698705500000FM 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Gluceofine Pro Blutentnahme-Lanzetten by Taidoc Technology Corporation — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TW-MF-000017956
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 094a0cb8-a8e8-4760-8b45-3ac2f94ddb71 61 fields · synced Sep 30, 2026