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GKS PRIME FLEX: TRAY n° 1 INOX supp. - Generic Instruments

EUDAMED

Class I (EU MDR)

Ref S50280

by Permedica S.p.A

Identity

Trade Name
GKS PRIME FLEX: TRAY n° 1 INOX supp. - Generic Instruments EUDAMED
Device Name
Instruments Tray EUDAMED
Model / Reference
S50280 EUDAMED

Identifiers

Primary DI / UDI-DI
08050323168262 EUDAMED
Basic UDI-DI
8050323I0001AZV EUDAMED
Direct Marketing DI
08050323168262 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

Category: Instrument tray, reusable

GKS PRIME FLEX: TRAY n° 1 INOX supp. - Generic Instruments by Permedica S.p.A — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

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 1eb02b3a-b97b-4ecf-b5ae-fbb6e158b138 61 fields · synced Jun 19, 2026