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Pulp kidney dish

EUDAMED

Class I (EU MDR)

Ref 7050BModel FN-KD02Ref KEY001

by Finess Healthcare Group Co., Ltd

Identity

Trade Name
Pulp kidney dish EUDAMED
Device Name
Kidney Dish EUDAMED
Model / Reference
FN-KD02 EUDAMED
7050B EUDAMED
KEY001 EUDAMED

Identifiers

Primary DI / UDI-DI
06973911698830 EUDAMED
06973911697703 EUDAMED
Basic UDI-DI
697391169KD02LL EUDAMED
EMDN Code
V0402 CLINICAL USE TRAYS AND BOWLS EUDAMED

Classification

Device Class
Class I 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

Pulp kidney dish by Finess Healthcare Group Co., Ltd — Class I — 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
CN-MF-000004124
Authorised Representative
Zoustech S.L. ES-AR-000002008

Sources (2)

  • EUDAMED 50d2bb0b-c44d-4883-b375-2875759cbb2a 61 fields · synced Oct 6, 2026
  • EUDAMED a6b3317f-e096-4e25-a15a-a94fe2db8649 61 fields · synced May 18, 2026