← Back to catalogue

Drivemedical

FDA UDI

Class I (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
PowerAccessories Product Description: Sun Shade for Scooter,1/ea FDA UDI
Model / Reference
SL18 FDA UDI
Description
PowerAccessories Product Description: Sun Shade for Scooter,1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00822383124230 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Electric-motor-driven wheelchair, attendant-controlled 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: Electric-motor-driven wheelchair, attendant-controlled

Drivemedical by Drive Devilbiss Healthcare — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 2539bf72-cb01-40a4-8624-0f62c6191f23 33 fields · synced Jun 8, 2026