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Osteotrans

EUDAMED

Class III (EU MDR)

Ref RK0720

by Teijin Medical Technologies Co., Ltd.

Identity

Trade Name
OSTEOTRANS EUDAMED
Device Name
BioactIF OSTEOTRANS EUDAMED
Model / Reference
RK0720 EUDAMED

Identifiers

Primary DI / UDI-DI
04550052844450 EUDAMED
Basic UDI-DI
B-04550052844450 EUDAMED
EMDN Code
P09120605 INTERFERENCE SCREWS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Osteotrans by Teijin Medical Technologies Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/MDD

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Manufacturer

EUDAMED SRN
JP-MF-000032429
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 0a98d67f-4d2f-4a06-9aad-1e5a1b05f8b2 61 fields · synced Jun 19, 2026