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Acto Oxy Foam 1 L

EUDAMED

Class IIa (EU MDR)

Ref 05.5710.1Model Acto Oxy Foam 1 L

by ACTO GmbH

Identity

Trade Name
Acto Oxy Foam 1 L EUDAMED
Device Name
Medical Device Surface Disinfectant EUDAMED
Model / Reference
Acto Oxy Foam 1 L EUDAMED
05.5710.1 EUDAMED

Identifiers

Primary DI / UDI-DI
04250108357124 EUDAMED
Basic UDI-DI
B-04250108357124 EUDAMED
EMDN Code
D0502 HYDROGEN PEROXIDE FOR DISINFECTION OF MEDICAL DEVICES EUDAMED

Classification

Device Class
Class IIa 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

No

EUDAMED

Acto Oxy Foam 1 L by ACTO GmbH — Class IIa — 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 ca7fd928-e057-4bac-b414-f5a750efbc4c 61 fields · synced Oct 6, 2026