Identity
- Trade Name
- Maxi Air EUDAMED
- Device Name
- Maxi Air EUDAMED
- Model / Reference
- MAS000001-DE EUDAMEDMAS000001-EU EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055982794534 EUDAMED
- Basic UDI-DI
- 5060693520297WS EUDAMED
- EMDN Code
- Z12019010 PATIENT TRANSFER SYSTEMS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Ireland 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 (1)
- EUDAMED 8f6ee271-0482-42c9-8cbc-865629e7eede 61 fields · synced May 29, 2026