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Footswitch

EUDAMED

Class I (EU MDR)

Ref 7-PG1-132

by Creo Medical

Identity

Device Name
Footswitch EUDAMED
Model / Reference
7-PG1-132 EUDAMED

Identifiers

Primary DI / UDI-DI
05060359560100 EUDAMED
Basic UDI-DI
506035956FootswitchPG1YR EUDAMED
Direct Marketing DI
05060359560100 EUDAMED
EMDN Code
Z12010980 ELECTROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

Footswitch by Creo Medical — 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
Creo Medical
EUDAMED SRN
GB-MF-000019076
Authorised Representative
Creo Medical, S.L.U. ES-AR-000001355

Sources (1)

  • EUDAMED 8be10bb3-1efa-439d-9a6a-40dd06dd6808 61 fields · synced Jul 15, 2026