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Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Drive FDA UDI
Generic Name
Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI
Device Name
Junior Swing Ft.Rest,Tool Free,Viper,1pr FDA UDI
Model / Reference
JL3-4SF-TF FDA UDI
Description
Junior Swing Ft.Rest,Tool Free,Viper,1pr FDA UDI

Identifiers

Primary DI / UDI-DI
00822383240367 FDA UDI
FDA Product Code
IMM FDA UDI
GMDN Term
Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible

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

Similar devices

Also classified as Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d74d30f2-d7cb-4655-92f0-fc4480c658b9 33 fields · synced Jun 8, 2026