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Footrise

EUDAMED

Class I (EU MDR)

Ref PO 31802

by Lomed Nederland

Identity

Trade Name
Footrise EUDAMED
Device Name
Pro Orthic Footrise EUDAMED
Model / Reference
PO 31802 EUDAMED

Identifiers

Primary DI / UDI-DI
08718873005733 EUDAMED
Basic UDI-DI
871887300573LC EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT 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

Category: Ankle/foot orthosis

Footrise by Lomed Nederland — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

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 8bb522c7-f37b-4a9f-a211-654f825e2257 61 fields · synced Jun 19, 2026