← Back to catalogue

Stiefel Curette

EUDAMED

Class IIa (EU MDR)

Ref 70592

by GlaxoSmithKline Trading Services Limited

Identity

Trade Name
Stiefel Curette EUDAMED
Device Name
Curette EUDAMED
Model / Reference
70592 EUDAMED

Identifiers

Primary DI / UDI-DI
85054363000321 EUDAMED
Basic UDI-DI
5054363591471876DH EUDAMED
EMDN Code
A01020303 CUTANEOUS BIOPSY CURETTES, 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

Category: Dermal curette, single-use

Stiefel Curette by GlaxoSmithKline Trading Services Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dermal curette, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IE-MF-000008351

Sources (1)

  • EUDAMED b94fe3fd-49c2-4174-83c7-ffa513cfee6e 61 fields · synced Jun 20, 2026