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Actosept AF Plus 500 ml

EUDAMED

Class IIa (EU MDR)

Ref 05.4849.500Model Actosept AF Plus 500 ml

by ACTO GmbH

Identity

Trade Name
Actosept AF Plus 500 ml EUDAMED
Device Name
Medical Device Surface Disinfectant EUDAMED
Model / Reference
Actosept AF Plus 500 ml EUDAMED
05.4849.500 EUDAMED

Identifiers

Primary DI / UDI-DI
04250108348412 EUDAMED
Basic UDI-DI
B-04250108348412 EUDAMED
EMDN Code
D0799 ALCOHOLS FOR THE DISINFECTION OF MEDICAL DEVICES - OTHER 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

Actosept AF Plus 500 ml 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 acb4736b-69cc-4533-952f-6ee22e91c5a9 61 fields · synced Oct 6, 2026