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DERMAL CURETTE 5mm

EUDAMED

Class IIa (EU MDR)

Ref 50105

by Kai Industries Co., Ltd.

Identity

Trade Name
DERMAL CURETTE 5mm EUDAMED
DERMAL CURETTE EUDAMED
Device Name
DERMAL CURETTE EUDAMED
Model / Reference
50105 EUDAMED

Identifiers

Primary DI / UDI-DI
04562143740244 EUDAMED
Basic UDI-DI
456014692AC014T 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

Yes

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

DERMAL CURETTE 5mm by Kai Industries Co., Ltd. — 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

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Manufacturer

EUDAMED SRN
JP-MF-000016663
Authorised Representative
Kai Europe GmbH DE-AR-000005096

Sources (2)

  • EUDAMED f26589d2-00ca-4fe0-bb14-9eef995c5766 61 fields · synced Jun 19, 2026
  • EUDAMED 7b83413f-2ef5-446e-8c39-f616d04adc06 61 fields · synced Jun 19, 2026