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Actosed Forte Ready 100 ml

EUDAMED

Class IIb (EU MDR)

Ref 01.0303.100Model Actosed Forte Ready 100 ml

by ACTO GmbH

Identity

Trade Name
Actosed Forte Ready 100 ml EUDAMED
Device Name
Invasive Medical Device Disinfectant EUDAMED
Model / Reference
Actosed Forte Ready 100 ml EUDAMED
01.0303.100 EUDAMED

Identifiers

Primary DI / UDI-DI
04250108303053 EUDAMED
Basic UDI-DI
B-04250108303053 EUDAMED
EMDN Code
D01010103 GLUTARALDEHYDE, NEUTRAL SOLUTION 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 Forte Ready 100 ml 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 a6fedd29-65be-405a-be47-5496b6bbc07d 61 fields · synced Oct 6, 2026