← Back to catalogue

Activa Instrument

EUDAMED

Class I (EU MDR)

Ref B-IS-9032

by Bioretec Ltd.

Identity

Trade Name
Activa Instrument EUDAMED
HEX shaft, for 2.0/2.7/3.5 mm screws EUDAMED
Device Name
HEX shaft, for 2.0/2.7/3.5 mm screws EUDAMED
Hex Driver EUDAMED
Model / Reference
B-IS-9032 EUDAMED

Identifiers

Primary DI / UDI-DI
06438394003347 EUDAMED
Basic UDI-DI
B-06438394003347 EUDAMED
6438394INS012WK EUDAMED
Direct Marketing DI
06438394003347 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bioretec Ltd.
EUDAMED SRN
FI-MF-000001328

Sources (2)

  • EUDAMED 6fa53428-e2f7-490b-b04f-3a3f40bb8c6d 61 fields · synced Aug 2, 2026
  • EUDAMED 034c7146-cad7-47df-9e5d-a54295ab9bf9 61 fields · synced May 18, 2026