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Actoton SN 5 L

EUDAMED

Class I (EU MDR)

Ref 04.1501.5Model Actoton A

by ACTO GmbH

Identity

Trade Name
Actoton SN 5 L EUDAMED
Device Name
Medical Device Neutralising Agent EUDAMED
Model / Reference
Actoton A EUDAMED
04.1501.5 EUDAMED

Identifiers

Primary DI / UDI-DI
04250108315018 EUDAMED
Basic UDI-DI
4250108304.MDNA.01LW EUDAMED
Direct Marketing DI
04250108315018 EUDAMED
EMDN Code
D0801 ENZYMATIC DETERGENTS FOR MEDICAL DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Actoton SN 5 L by ACTO GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ACTO GmbH
EUDAMED SRN
DE-MF-000019128

Sources (1)

  • EUDAMED ba154069-9bac-46da-8aad-b29868363708 61 fields · synced Oct 6, 2026