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Actilite

EUDAMED

Class IIb (EU MDR)

Ref CR4367

by Brightwake Limited

Identity

Trade Name
Actilite EUDAMED
Device Name
Actilite EUDAMED
Model / Reference
CR4367 EUDAMED

Identifiers

Primary DI / UDI-DI
05060031479928 EUDAMED
Basic UDI-DI
B-05060031479928 EUDAMED
EMDN Code
M040499 DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Ireland 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

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Actilite by Brightwake Limited — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

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 (1)

  • EUDAMED 13610853-7a65-4bde-8c57-f3a7ef3c4409 61 fields · synced Jun 18, 2026