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Maxi Air

FDA UDI

Class I (US FDA UDI)

by Arjohuntleigh, Inc.

Identity

Trade Name
Maxi Air FDA UDI
Generic Name
Patient lifting system stretcher FDA UDI
Device Name
Maxi Air Transfer Mattress, 34" LATERAL L FDA UDI
Model / Reference
MAS14000-US FDA UDI
Description
Maxi Air Transfer Mattress, 34" LATERAL L FDA UDI

Identifiers

Primary DI / UDI-DI
05056341675709 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

Maxi Air 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 3f8b7690-dedb-410d-b21c-e02282a28e3f 33 fields · synced Jun 6, 2026