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Φουστα Νοσηλειας S

EUDAMED

Class I (EU MDR)

Ref M510000SModel ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ L

by Αντιγονη Πετροπουλου Και Σια Οε

Identity

Trade Name
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ S EUDAMED
Device Name
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ EUDAMED
Model / Reference
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ L EUDAMED
M510000S EUDAMED

Identifiers

Primary DI / UDI-DI
05207356000875 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 S 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 67839721-dd76-4a94-ae4a-40017b7d67ca 61 fields · synced Jun 18, 2026