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Double-ended dermal curette

EUDAMED

Class IIa (EU MDR)

Ref 50755Model 3406

by Laboratoires PAUL HARTMANN S.à.r.l

Identity

Device Name
Double-ended dermal curette EUDAMED
Model / Reference
3406 EUDAMED
50755 EUDAMED

Identifiers

Primary DI / UDI-DI
03261480004811 EUDAMED
Basic UDI-DI
32614834064W EUDAMED
Direct Marketing DI
03261480004811 EUDAMED
EMDN Code
V0199 CUTTING DEVICES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

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: Cranial bur, single-use

Double-ended dermal curette by Laboratoires PAUL HARTMANN S.à.r.l — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cranial bur, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
FR-MF-000004029

Sources (1)

  • EUDAMED 52aba5f1-b615-4c66-9d0b-8ee5637e1a61 61 fields · synced Jun 18, 2026