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Actosept AF 750 ml
EUDAMEDClass IIa (EU MDR)
Ref 05.2301.750Model Actosept AF 750 ml
by ACTO GmbH
Identity
- Trade Name
- Actosept AF 750 ml EUDAMED
- Device Name
- Medical Device Surface Disinfectant EUDAMED
- Model / Reference
- Actosept AF 750 ml EUDAMED05.2301.750 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250108323044 EUDAMED
- Basic UDI-DI
- B-04250108323044 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 750 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04250108323044 | Class IIa | Active |
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Manufacturer
- Manufacturer
- ACTO GmbH
- EUDAMED SRN
- DE-MF-000019128
Sources (1)
- EUDAMED ee26d340-1411-4c78-8a41-f83d7d07c432 61 fields · synced Oct 6, 2026