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Activa IM-Nail™

EUDAMED

Class III (EU MDR)

Ref B-ANIM-32400

by Bioretec Ltd.

Identity

Trade Name
Activa IM-Nail™ EUDAMED
Device Name
Activa IM-Nail™ 3.2 x 400 mm EUDAMED
Model / Reference
B-ANIM-32400 EUDAMED

Identifiers

Primary DI / UDI-DI
06438394007307 EUDAMED
Basic UDI-DI
B-06438394007307 EUDAMED
EMDN Code
P09120201 INTRAMEDULLARY NAILS 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

Activa IM-Nail™ 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 d5607d2b-806d-4e04-b819-56f4ea6a97d2 61 fields · synced Jun 19, 2026