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ActivaScrew™ Interference TCP

EUDAMED

Class III (EU MDR)

Ref B-DI-0930

by Bioretec Ltd.

Identity

Trade Name
ActivaScrew™ Interference TCP EUDAMED
Device Name
ActivaScrew™ Interference TCP 9 x 30 mm EUDAMED
Model / Reference
B-DI-0930 EUDAMED

Identifiers

Primary DI / UDI-DI
06438394011878 EUDAMED
Basic UDI-DI
B-06438394011878 EUDAMED
EMDN Code
P09120605 INTERFERENCE SCREWS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Finland 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

ActivaScrew™ Interference TCP by Bioretec 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 Active

CE/MDD

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Manufacturer

Manufacturer
Bioretec Ltd.
EUDAMED SRN
FI-MF-000001328

Sources (1)

  • EUDAMED 4155c47c-ab94-48a2-b05f-2526d1ed1e50 61 fields · synced Jun 18, 2026