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Medial Rotation Knee

EUDAMED

Class III (EU MDR)

Ref 156-111Model Medial Rotation Knee

by MatOrtho Limited

Identity

Trade Name
Medial Rotation Knee EUDAMED
Device Name
Medial Rotation Knee Femur EUDAMED
Model / Reference
Medial Rotation Knee EUDAMED
156-111 EUDAMED

Identifiers

Primary DI / UDI-DI
05055455503502 EUDAMED
Basic UDI-DI
B-05055455503502 EUDAMED
EMDN Code
P0909030101 BICOMPARTMENTAL PRIMARY IMPLANT CEMENTED FEMORAL COMPONENTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Medial Rotation Knee by MatOrtho Limited — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
MatOrtho Limited
EUDAMED SRN
GB-MF-000007614
Authorised Representative
MatOrtho Ireland Limited IE-AR-000006856

Sources (1)

  • EUDAMED d2be5fa0-f7cb-430d-9cd2-bfee5d62881c 61 fields · synced Jun 19, 2026