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ActivaPin™

EUDAMED

Class III (EU MDR)

Ref B-AP-3270

by Bioretec Ltd.

Identity

Trade Name
ActivaPin™ EUDAMED
Device Name
ActivaPin™ 3.2mm x 70 mm EUDAMED
Model / Reference
B-AP-3270 EUDAMED

Identifiers

Primary DI / UDI-DI
06438394000216 EUDAMED
Basic UDI-DI
B-06438394000216 EUDAMED
EMDN Code
P09120606 OSTEOSYNTHESIS DEVICES, BIODEGRADABLE SCREWS AND BARS 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

ActivaPin™ by Bioretec Ltd. — 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

Manufacturer
Bioretec Ltd.
EUDAMED SRN
FI-MF-000001328

Sources (1)

  • EUDAMED ab0d0977-063f-47c9-9667-fed5919a9d27 61 fields · synced May 23, 2026