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Patella

EUDAMED

Class III (EU MDR)

Ref 135250035S

by Double Medical Technology Inc.

Identity

Device Name
Patella EUDAMED
Model / Reference
135250035S EUDAMED

Identifiers

Primary DI / UDI-DI
06902139322135 EUDAMED
Basic UDI-DI
B-06902139322135 EUDAMED
EMDN Code
P0909070201 PATELLAR COMPONENTS, MONOBLOCK EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Croatia 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

Patella by Double Medical Technology Inc. — 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

EUDAMED SRN
CN-MF-000009048
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 36ba30db-268c-4b21-a30b-94e01c2eb30f 61 fields · synced Jul 26, 2026