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Activa Instrument

EUDAMED

Class I (EU MDR)

Ref B-ISC-4502

by Bioretec Ltd.

Identity

Trade Name
Activa Instrument EUDAMED
Direct driver, for 4.0/4.5 mm cannulated screws EUDAMED
Device Name
Direct driver, for 4.0/4.5 mm cannulated screws EUDAMED
Direct Driver EUDAMED
Model / Reference
B-ISC-4502 EUDAMED

Identifiers

Primary DI / UDI-DI
06438394005235 EUDAMED
Basic UDI-DI
B-06438394005235 EUDAMED
6438394INS009WW EUDAMED
Direct Marketing DI
06438394005235 EUDAMED
EMDN Code
L26 SURGICAL SCREWDRIVERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Surgical screwdriver, reusable

Activa Instrument by Bioretec Ltd. — Class I — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Bioretec Ltd.
EUDAMED SRN
FI-MF-000001328

Sources (2)

  • EUDAMED 9de8e606-442d-4611-9540-1ec090f04b70 61 fields · synced Jul 14, 2026
  • EUDAMED b7c3c734-6026-4e35-9d41-e114e45ac00d 61 fields · synced May 19, 2026