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Actosed Forte Ready 1 L
EUDAMEDClass IIb (EU MDR)
Ref 01.0303.1Model Actosed Forte Ready 1 L
by ACTO GmbH
Identity
- Trade Name
- Actosed Forte Ready 1 L EUDAMED
- Device Name
- Invasive Medical Device Disinfectant EUDAMED
- Model / Reference
- Actosed Forte Ready 1 L EUDAMED01.0303.1 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250108303046 EUDAMED
- Basic UDI-DI
- B-04250108303046 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 1 L 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04250108303046 | Class IIb | Active |
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Manufacturer
- Manufacturer
- ACTO GmbH
- EUDAMED SRN
- DE-MF-000019128
Sources (1)
- EUDAMED 77389ab2-8104-4858-a697-e3cb560ae299 61 fields · synced Oct 6, 2026