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Wound Probe

EUDAMED

Class I (EU MDR)

Ref CR4236Ref CR4223

by Brightwake Limited

Identity

Trade Name
Wound Probe EUDAMED
Device Name
Wound Probe EUDAMED
Model / Reference
CR4236 EUDAMED
CR4223 EUDAMED

Identifiers

Primary DI / UDI-DI
05060031476798 EUDAMED
05060031476712 EUDAMED
Basic UDI-DI
B-05060031476798 EUDAMED
B-05060031476712 EUDAMED
EMDN Code
Z120499 GENERAL MEDICINE INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Wound Probe by Brightwake Limited — Class I — 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
Brightwake Limited
EUDAMED SRN
GB-MF-000012039
Authorised Representative
CS Life Sciences Europe Ltd IE-AR-000004113

Sources (2)

  • EUDAMED fdf926d1-4e6f-4681-a893-db87cd4c1eb4 61 fields · synced Jul 26, 2026
  • EUDAMED 75d41af4-ad47-443e-97ef-fef870c0e135 61 fields · synced May 18, 2026