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Maxi Air
EUDAMEDClass I (EU MDR)
Ref MAS000001-DKModel MAS000001-DERef MAS000001-SE
Identity
- Trade Name
- Maxi Air EUDAMED
- Device Name
- Maxi Air EUDAMED
- Model / Reference
- MAS000001-DE EUDAMEDMAS000001-DK EUDAMEDMAS000001-SE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055982794527 EUDAMED05055982794596 EUDAMED
- Basic UDI-DI
- 5060693520297WS EUDAMED
- EMDN Code
- Z12019010 PATIENT TRANSFER SYSTEMS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Denmark EUDAMEDSweden 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
Maxi Air by Arjohuntleigh AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5060693520297WS | Class I | Active |
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Manufacturer
- Manufacturer
- ArjoHuntleigh AB
- EUDAMED SRN
- SE-MF-000000696
Sources (2)
- EUDAMED b59af123-1247-4121-846c-5329ebb51f89 61 fields · synced Sep 17, 2026
- EUDAMED 9cd195e2-0245-4d3e-aa01-74aa1a5e512d 61 fields · synced May 18, 2026