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Actolind w Solution 5x10 ml

EUDAMED

Class III (EU MDR)

Ref 06.6703.10MModel Actolind w Solution 5x10 ml

by ACTO GmbH

Identity

Trade Name
Actolind w Solution 5x10 ml EUDAMED
Device Name
Wound Care Solution EUDAMED
Model / Reference
Actolind w Solution 5x10 ml EUDAMED
06.6703.10M EUDAMED

Identifiers

Primary DI / UDI-DI
04250108306702 EUDAMED
Basic UDI-DI
B-04250108306702 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 Solution 5x10 ml by ACTO GmbH — Class III — 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
ACTO GmbH
EUDAMED SRN
DE-MF-000019128

Sources (1)

  • EUDAMED bac3942c-6b7e-455d-b8ef-fcc44763d10b 61 fields · synced Oct 6, 2026