← Back to catalogue

Φουστα Νοσηλειας Xs

EUDAMED

Class I (EU MDR)

Ref M510000XSModel ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ L

by Αντιγονη Πετροπουλου Και Σια Οε

Identity

Trade Name
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ XS EUDAMED
Device Name
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ EUDAMED
Model / Reference
ΦΟΥΣΤΑ ΝΟΣΗΛΕΙΑΣ L EUDAMED
M510000XS EUDAMED

Identifiers

Primary DI / UDI-DI
05207356000899 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 Xs 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
GR-MF-000019297

Sources (1)

  • EUDAMED 533664fb-d66f-478a-91f1-3c0a659980ec 61 fields · synced Jul 8, 2026