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Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVE FDA UDI
Generic Name
Freestanding patient lifting system, electrically-powered FDA UDI
Device Name
Patient Room Lifts Product Description Digital Scale,HD 600 LB Lift,1/ea FDA UDI
Model / Reference
13046-HD FDA UDI
Description
Patient Room Lifts Product Description Digital Scale,HD 600 LB Lift,1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00822383255521 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Freestanding 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

No

FDA UDI

Category: Freestanding patient lifting system, electrically-powered

Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 0c633f78-ff35-42d3-a4be-82c0a8bdcff8 33 fields · synced Jun 8, 2026