← Back to catalogue

Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI
Device Name
Transport/WheelchairWheelchairs K6 Product Description: Sentra EC,26in Det.FullArm,1/cs FDA UDI
Model / Reference
STD26ECDFA FDA UDI
Description
Transport/WheelchairWheelchairs K6 Product Description: Sentra EC,26in Det.FullArm,1/cs FDA UDI

Identifiers

Primary DI / UDI-DI
00822383137230 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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

Yes

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

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

Drivemedical 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

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

Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 685e3c0e-d674-44cd-997c-06673ec4c048 33 fields · synced Jun 8, 2026