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Activa Instrument

EUDAMED

Class IIa (EU MDR)

Ref B-II-1630BModel B-II-1624B

by Bioretec Ltd.

Identity

Trade Name
Activa Instrument EUDAMED
Device Name
K-wire Ø1.6 mm, length 240 mm, blunt ends, for 7/8/9/10/11 mm interference screw EUDAMED
Model / Reference
B-II-1624B EUDAMED
B-II-1630B EUDAMED

Identifiers

Primary DI / UDI-DI
06438394009189 EUDAMED
Basic UDI-DI
B-06438394009189 EUDAMED
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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 Instrument by Bioretec Ltd. — Class IIa — 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 ba09e77b-cdc5-4365-8614-7a8a72dbf88d 61 fields · synced May 22, 2026