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GKS PRIME FLEX: TRAY n° 2 INOX supp. - Generic Instruments

EUDAMED

Class I (EU MDR)

Ref S50281

by Permedica S.p.A

Identity

Trade Name
GKS PRIME FLEX: TRAY n° 2 INOX supp. - Generic Instruments EUDAMED
Device Name
Instruments Tray EUDAMED
Model / Reference
S50281 EUDAMED

Identifiers

Primary DI / UDI-DI
08050323168279 EUDAMED
Basic UDI-DI
8050323I0001AZV EUDAMED
Direct Marketing DI
08050323168279 EUDAMED
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

GKS PRIME FLEX: TRAY n° 2 INOX supp. - Generic Instruments by Permedica S.p.A — 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

Manufacturer
Permedica S.p.A
EUDAMED SRN
IT-MF-000008110

Sources (1)

  • EUDAMED 3150846b-2caa-4bd5-b7f1-5b7f9d2477ef 61 fields · synced Sep 17, 2026