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Drivemedical

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Electric-motor-driven wheelchair, attendant-controlled FDA UDI
Device Name
Parts Product Description: 50AH Battery w Box, Cirrus Plus 24",2/ FDA UDI
Model / Reference
CPLUSBATT-50 FDA UDI
Description
Parts Product Description: 50AH Battery w Box, Cirrus Plus 24",2/ FDA UDI

Identifiers

Primary DI / UDI-DI
00822383969916 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, attendant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric-motor-driven wheelchair, attendant-controlled

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

Similar devices

Also classified as Electric-motor-driven wheelchair, attendant-controlled.

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 416cfe82-ab13-4584-9907-7a939b57733f 33 fields · synced Jun 8, 2026