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Maxi 500

FDA UDI

Class I (US FDA UDI)

by Arjohuntleigh, Inc.

Identity

Trade Name
Maxi 500 FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
Maxi 500 Manual DPS w/Scale - Mobile Floor Lifter - Safe working load of 500 lb / 227 kg FDA UDI
Model / Reference
KM560180 FDA UDI
Description
Maxi 500 Manual DPS w/Scale - Mobile Floor Lifter - Safe working load of 500 lb / 227 kg FDA UDI

Identifiers

Primary DI / UDI-DI
05056097358741 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mobile patient lifting system, electrically-powered

Maxi 500 by Arjohuntleigh, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile patient lifting system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arjohuntleigh, Inc.

Sources (1)

  • FDA UDI cff29a25-324c-434b-92e2-f3373113849d 33 fields · synced Jun 6, 2026