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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Attendant-only-propelled wheelchair, non-bariatric FDA UDI
Model / Reference
CW0006CS FDA UDI

Identifiers

Catalog Number
CW0006CS FDA UDI
Primary DI / UDI-DI
50885380046245 FDA UDI
510(k) Number
K051481 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Attendant-only-propelled wheelchair, non-bariatric 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Attendant-only-propelled wheelchair, non-bariatric

A comprehensive 2-3 paragraph SEO description for the Cardinal Health Attendant-only-propelled wheelchair, a non-bariatric mobility device designed to transport individuals without full walking capacity.

Similar devices

Also classified as Attendant-only-propelled wheelchair, non-bariatric.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fe24b137-626a-49b4-be78-d356972bdac0 34 fields · synced Jul 22, 2026