← Back to catalogue

Osteotrans

EUDAMED

Class III (EU MDR)

Ref RK0925

by Teijin Medical Technologies Co., Ltd.

Identity

Trade Name
OSTEOTRANS EUDAMED
Device Name
BioactIF OSTEOTRANS EUDAMED
Model / Reference
RK0925 EUDAMED

Identifiers

Primary DI / UDI-DI
04550052844528 EUDAMED
Basic UDI-DI
B-04550052844528 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European Union No Longer Active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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED a7a58806-49ec-4bee-9311-aaa20eabe6d8 61 fields · synced Jun 19, 2026