← Back to catalogue
Acto Oxy Foam 750 ml
EUDAMEDClass IIa (EU MDR)
Ref 05.5710.750Model Acto Oxy Foam 750 ml
by ACTO GmbH
Identity
- Trade Name
- Acto Oxy Foam 750 ml EUDAMED
- Device Name
- Medical Device Surface Disinfectant EUDAMED
- Model / Reference
- Acto Oxy Foam 750 ml EUDAMED05.5710.750 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250108357117 EUDAMED
- Basic UDI-DI
- B-04250108357117 EUDAMED
- EMDN Code
- D0502 HYDROGEN PEROXIDE FOR DISINFECTION OF MEDICAL DEVICES 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
Acto Oxy Foam 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-04250108357117 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- ACTO GmbH
- EUDAMED SRN
- DE-MF-000019128
Sources (1)
- EUDAMED e8b1f475-c2c7-4621-bb99-2bb599c0c2d8 61 fields · synced Oct 6, 2026