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Actolind w Gel 50 ml

EUDAMED

Class III (EU MDR)

Ref 06.6803.50Model Actolind w Gel 50 ml

by ACTO GmbH

Identity

Trade Name
Actolind w Gel 50 ml EUDAMED
Device Name
Wound Care Gel EUDAMED
Model / Reference
Actolind w Gel 50 ml EUDAMED
06.6803.50 EUDAMED

Identifiers

Primary DI / UDI-DI
04250108306849 EUDAMED
Basic UDI-DI
B-04250108306849 EUDAMED
EMDN Code
M040412 ANTISEPTICS-BASED DRESSINGS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Yes

EUDAMED

Actolind w Gel 50 ml by ACTO GmbH — Class III — CE/MDR — 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
ACTO GmbH
EUDAMED SRN
DE-MF-000019128

Sources (1)

  • EUDAMED ad686f6f-4393-4e14-87b3-4e9fa155e479 61 fields · synced Oct 7, 2026