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Actosed PA Powder 810 g

EUDAMED

Class IIb (EU MDR)

Ref 01.9605.810Model Actosed PA Powder 810 g

by ACTO GmbH

Identity

Trade Name
Actosed PA Powder 810 g EUDAMED
Device Name
Invasive Medical Device Disinfectant EUDAMED
Model / Reference
Actosed PA Powder 810 g EUDAMED
01.9605.810 EUDAMED

Identifiers

Primary DI / UDI-DI
04250108396062 EUDAMED
Basic UDI-DI
B-04250108396062 EUDAMED
EMDN Code
D050103 PERACETIC ACID FOR THE DISINFECTION OF MEDICAL DEVICES EUDAMED

Classification

Device Class
Class IIb 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

Actosed PA Powder 810 g by ACTO GmbH — Class IIb — 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 79651fd2-ed5a-488d-9f0a-cd295666991f 61 fields · synced Oct 6, 2026