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PP/PE-Schutzkittel

EUDAMED

Class I (EU MDR)

Ref 70210Model FN-IG0102

by Finess Healthcare Group Co., Ltd

Identity

Trade Name
PP/PE-Schutzkittel EUDAMED
Device Name
Isolation Gown EUDAMED
Model / Reference
FN-IG0102 EUDAMED
70210 EUDAMED

Identifiers

Primary DI / UDI-DI
06978486830050 EUDAMED
Basic UDI-DI
697391169IG0102DG EUDAMED
EMDN Code
T0205 NON-SURGICAL GOWNS (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

PP/PE-Schutzkittel 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 (1)

  • EUDAMED eb69d73c-03ba-4053-b12e-4b2a10c252b3 61 fields · synced Oct 6, 2026