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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
DBD-LIFT,PATIENT,ELECTRIC,500LB CAPACITY FDA UDI
Model / Reference
MDS500EL FDA UDI
Description
DBD-LIFT,PATIENT,ELECTRIC,500LB CAPACITY FDA UDI

Identifiers

Catalog Number
MDS500EL FDA UDI
Primary DI / UDI-DI
10888277660540 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mobile patient lifting system, electrically-powered

Medline by Medline Industries, 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
Medline Industries, Inc.

Sources (1)

  • FDA UDI 38347eee-3346-4b11-923f-ee4ec84617ec 35 fields · synced May 30, 2026