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Stiefel Curette

EUDAMED

Class IIa (EU MDR)

Ref 61569

by GlaxoSmithKline Trading Services Limited

Identity

Trade Name
Stiefel Curette EUDAMED
Device Name
Curette EUDAMED
Model / Reference
61569 EUDAMED

Identifiers

Primary DI / UDI-DI
85054363000314 EUDAMED
Basic UDI-DI
5054363591471876DH EUDAMED
EMDN Code
A01020303 CUTANEOUS BIOPSY CURETTES, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Stiefel Curette by GlaxoSmithKline Trading Services Limited — 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
IE-MF-000008351

Sources (1)

  • EUDAMED e420549e-e54a-4f3a-b672-0aaf8fce1c20 61 fields · synced Jun 18, 2026