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Φουστα Νοσηλειας M

EUDAMED

Class I (EU MDR)

Ref Μ510000ΜModel ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ L

by Αντιγονη Πετροπουλου Και Σια Οε

Identity

Trade Name
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ M EUDAMED
Device Name
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ EUDAMED
Model / Reference
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ L EUDAMED
Μ510000Μ EUDAMED

Identifiers

Primary DI / UDI-DI
05207356000868 EUDAMED
Basic UDI-DI
5207356000851U6 EUDAMED
EMDN Code
T0205 NON-SURGICAL GOWNS (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Φουστα Νοσηλειας M by Αντιγονη Πετροπουλου Και Σια Οε — 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
GR-MF-000019297

Sources (1)

  • EUDAMED 423eec5c-ea98-47cd-82fa-59a3dee9700b 61 fields · synced Jul 8, 2026