← Back to catalogue

GKS PRIME FLEX: TRAY n° 3 INOX supp. - TIBIA TOP/MOBILE

EUDAMED

Class I (EU MDR)

Ref S50282

by Permedica S.p.A

Identity

Trade Name
GKS PRIME FLEX: TRAY n° 3 INOX supp. - TIBIA TOP/MOBILE EUDAMED
Device Name
Instruments Tray EUDAMED
Model / Reference
S50282 EUDAMED

Identifiers

Primary DI / UDI-DI
08050323168286 EUDAMED
Basic UDI-DI
8050323I0001AZV EUDAMED
Direct Marketing DI
08050323168286 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° 3 INOX supp. - TIBIA TOP/MOBILE 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

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

Manufacturer

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

Sources (1)

  • EUDAMED fb14379d-9666-4bed-8970-08b1d4f7b72d 61 fields · synced Jun 18, 2026