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Noviomagus Revision Mesh

EUDAMED

Class IIb (EU MDR)

Ref NRM-0906-PFModel Noviomagus Revision Mesh Proximal Femur

by Spierings Orthopaedics B.V.

Identity

Trade Name
Noviomagus Revision Mesh EUDAMED
Device Name
Noviomagus Revision Mesh Proximal Femur EUDAMED
Model / Reference
Noviomagus Revision Mesh Proximal Femur EUDAMED
NRM-0906-PF EUDAMED

Identifiers

Primary DI / UDI-DI
08720254007724 EUDAMED
Basic UDI-DI
B-08720254007724 EUDAMED
EMDN Code
P09088002 ACETABULAR MESHES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands 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

Noviomagus Revision Mesh by Spierings Orthopaedics B.V. — Class IIb — 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

EUDAMED SRN
NL-MF-000023199

Sources (1)

  • EUDAMED 04597fd5-b89e-466a-8722-b5f2ceb40233 61 fields · synced Jul 12, 2026