← Back to catalogue
LIFTKAR PT-Adapt 130
EUDAMEDFDA 510(k)Class I (EU MDR)
Ref 045721510(k) K111858
Identity
- Trade Name
- LIFTKAR PT-Adapt 130 EUDAMED
- Device Name
- Liftkar PT EUDAMED
- Model / Reference
- 045721 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 09120047770214 EUDAMED
- Basic UDI-DI
- 912004777PTS2 EUDAMED
- Direct Marketing DI
- 09120047770214 EUDAMED
- EMDN Code
- Y183012 MOBILE STAIRLIFTS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria 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
LIFTKAR PT-Adapt 130 by Sano Transportgeraete Gmbh — Class I — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K111858 | Class I | Active |
| FDA 510(k) | United States | FDA_510K | K110495 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 912004777PTS2 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sano Transportgeraete GmbH
- EUDAMED SRN
- AT-MF-000053609
Sources (3)
- EUDAMED d8a4d27f-1300-47fc-9d10-4b294e82627b 85 fields · synced Jun 19, 2026
- EUDAMED 0bb7bdad-5242-4bc8-a290-55bcca56615c 61 fields · synced Jun 19, 2026
- FDA 510(k) K111858 1 fields · synced May 18, 2026