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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Assistive scooter, electric-motor-driven FDA UDI
Device Name
Parts Product Description: Sdrivecontroller,PhoenixHD4, 1/EA FDA UDI
Model / Reference
C10-067-00200 FDA UDI
Description
Parts Product Description: Sdrivecontroller,PhoenixHD4, 1/EA FDA UDI

Identifiers

Primary DI / UDI-DI
00822383990897 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Assistive scooter, electric-motor-driven 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

No

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: Assistive scooter, electric-motor-driven

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

Similar devices

Also classified as Assistive scooter, electric-motor-driven.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI abe2a490-d131-44dd-8067-1a97210af40a 33 fields · synced Jun 8, 2026