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Silicone Heel Cup

EUDAMED

Class I (EU MDR)

Ref 5454DM-N2

by OPPO Medical Inc.

Identity

Trade Name
Silicone Heel Cup EUDAMED
Device Name
FOOT ORTHOSES EUDAMED
Model / Reference
5454DM-N2 EUDAMED

Identifiers

Primary DI / UDI-DI
00840270608960 EUDAMED
Basic UDI-DI
08402706CL1074X EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Silicone Heel Cup by OPPO Medical Inc. — 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
OPPO Medical Inc.
EUDAMED SRN
US-MF-000005202
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED df0df31a-ef2b-46f8-bced-a9485bf5e736 61 fields · synced Jun 19, 2026