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Airpal

FDA UDI

Class I (US FDA UDI)

by Arjohuntleigh, Inc.

Identity

Trade Name
AIRPAL FDA UDI
Generic Name
Patient lifting system stretcher FDA UDI
Device Name
AirPal launderable Long transfer mattress, 127 cm (50 in) FDA UDI
Model / Reference
AP-050N FDA UDI
Description
AirPal launderable Long transfer mattress, 127 cm (50 in) FDA UDI

Identifiers

Catalog Number
AP-050N FDA UDI
Primary DI / UDI-DI
05059441142485 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
MRI Safety
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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arjohuntleigh, Inc.

Sources (1)

  • FDA UDI 5af40c27-d791-401b-8346-c597a9ae25d2 35 fields · synced May 30, 2026