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Biopsy Punch

EUDAMED

Class IIa (EU MDR)

Ref LCH-PUK-50

by Kai Industries Co., Ltd.

Identity

Trade Name
BIOPSY PUNCH EUDAMED
Device Name
BIOPSY PUNCH EUDAMED
Model / Reference
LCH-PUK-50 EUDAMED

Identifiers

Primary DI / UDI-DI
04560146929024 EUDAMED
Basic UDI-DI
456014692AB014N EUDAMED
EMDN Code
A01020302 CUTANEOUS BIOPSY PUNCHES, 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

Biopsy Punch by Kai Industries Co., Ltd. — 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
JP-MF-000016663
Authorised Representative
Kai Europe GmbH DE-AR-000005096

Sources (1)

  • EUDAMED 9e571d24-dea9-45bf-83be-e6cde9738aba 61 fields · synced Aug 3, 2026