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Genu Airtex

EUDAMED

Class I (EU MDR)

Ref PO 31603-ES

by Lomed Nederland

Identity

Trade Name
Genu Airtex EUDAMED
Device Name
Genu Airtex EUDAMED
Model / Reference
PO 31603-ES EUDAMED

Identifiers

Primary DI / UDI-DI
08718873001155 EUDAMED
Basic UDI-DI
871887331603ES7V EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Genu Airtex by Lomed Nederland — 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
Lomed Nederland
EUDAMED SRN
NL-MF-000032807

Sources (1)

  • EUDAMED 81161df0-72c5-4629-b1d3-5bbbfd7dba45 61 fields · synced Jun 19, 2026