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TKA Pro

EUDAMED

Class IIa (EU MDR)

Ref L00002

by Blue Ortho SAS

Identity

Trade Name
TKA Pro EUDAMED
Device Name
TKA Pro EUDAMED
Model / Reference
L00002 EUDAMED

Identifiers

Primary DI / UDI-DI
10885862595843 EUDAMED
Basic UDI-DI
10885862100102NH EUDAMED
EMDN Code
Z12011482 SURGICAL NAVIGATION INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

TKA Pro by Blue Ortho SAS — Class IIa — 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
Blue Ortho SAS
EUDAMED SRN
FR-MF-000002436

Sources (1)

  • EUDAMED 2cd8a1f0-e63a-4a40-83b0-f213049b7507 61 fields · synced Jun 18, 2026