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Activa Instrument

EUDAMED

Class I (EU MDR)

Ref B-ISC-9033

by Bioretec Ltd.

Identity

Trade Name
Activa Instrument EUDAMED
HEX shaft, for 4.0/4.5 mm cannulated screws EUDAMED
Device Name
HEX shaft, for 4.0/4.5 mm cannulated screws EUDAMED
Hex Driver EUDAMED
Model / Reference
B-ISC-9033 EUDAMED

Identifiers

Primary DI / UDI-DI
06438394005211 EUDAMED
Basic UDI-DI
B-06438394005211 EUDAMED
6438394INS012WK EUDAMED
Direct Marketing DI
06438394005211 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 — MDD, MDR — 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/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Bioretec Ltd.
EUDAMED SRN
FI-MF-000001328

Sources (2)

  • EUDAMED 2363cc73-3348-4cd9-a896-8e9675abad91 61 fields · synced Jul 12, 2026
  • EUDAMED ae69dcf4-92ac-49c3-b52e-5abec889a98a 61 fields · synced May 17, 2026