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Heel cup - M

EUDAMED

Class I (EU MDR)

Ref PO 31311 MModel PO 31311

by Lomed Nederland

Identity

Trade Name
Heel cup - M EUDAMED
Device Name
Heel Cup EUDAMED
Model / Reference
PO 31311 EUDAMED
PO 31311 M EUDAMED

Identifiers

Primary DI / UDI-DI
08718873001575 EUDAMED
Basic UDI-DI
871887331311LL EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) 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: Orthotic insole, prefabricated, non-antimicrobial

Heel cup - M by Lomed Nederland — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

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 e271adc1-bd26-4904-aa8b-51b039058193 61 fields · synced Jul 10, 2026