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Osteotrans

EUDAMED

Class III (EU MDR)

Ref OK0730A

by Teijin Medical Technologies Co., Ltd.

Identity

Trade Name
OSTEOTRANS EUDAMED
Device Name
BioactIF OSTEOTRANS EUDAMED
Model / Reference
OK0730A EUDAMED

Identifiers

Primary DI / UDI-DI
04550052847529 EUDAMED
Basic UDI-DI
B-04550052847529 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

Category: Tendon/ligament bone anchor, non-bioabsorbable

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

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

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European Union No Longer Active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 d3aeba0d-d58f-405c-86d6-3f544377fc70 61 fields · synced Jun 19, 2026