Identity
- Trade Name
- AIRPAL FDA UDI
- Generic Name
- Patient lifting system stretcher FDA UDI
- Device Name
- AirPal Disposable Sling Mattress 39 inch FDA UDI
- Model / Reference
- AP-039SPSS-DR FDA UDI
- Description
- AirPal Disposable Sling Mattress 39 inch FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05059441218913 FDA UDI
- FDA Product Code
- FMR FDA UDI
- GMDN Term
- Patient lifting system stretcher FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6785 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Category: Patient lifting system stretcher
Airpal by Arjohuntleigh, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient lifting system stretcher.
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- Symphony™ — Qfix · Class II
- Transfer board — Mobilex A/S · Class I
- Powered Loading System (PLS) (Component) — LIFEPORT, LLC. · Class I
- INSTALLATION, POWER LOADING SYSTEM, CESSNA 680 * PLS — LIFEPORT, LLC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Arjohuntleigh, Inc.
Sources (1)
- FDA UDI a68d1da7-8d99-469b-adbf-af0823ebe4ec 33 fields · synced May 30, 2026