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Heel Cup

EUDAMED

Class I (EU MDR)

Ref EU05300-1Model EU5300

by Mediroyal Nordic AB

Identity

Trade Name
Heel Cup EUDAMED
Device Name
Heel Cup EUDAMED
Model / Reference
EU5300 EUDAMED
EU05300-1 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032900675 EUDAMED
Basic UDI-DI
73400329EU53004Q EUDAMED
Direct Marketing DI
07340032900675 EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Heel Cup by Mediroyal Nordic AB — 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
Mediroyal Nordic AB
EUDAMED SRN
SE-MF-000007821

Sources (1)

  • EUDAMED 9c499c75-313b-4453-be16-6234d8067bbe 61 fields · synced Jun 18, 2026