Chariot III

FDA UDI

Class I (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name: Chariot III FDA UDI
Generic Name: Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name: Chariot III 20 inch K3 Wheelchair w/ Removable Adjustable-Height Flip-Back Full Arms w/ Elevating Leg Rests w/ 300lb Wt-Cap. w/ Nylon Seat w/ Seat Extension FDA UDI
Model / Reference: WCK320AHFAELR FDA UDI
Description: Chariot III 20 inch K3 Wheelchair w/ Removable Adjustable-Height Flip-Back Full Arms w/ Elevating Leg Rests w/ 300lb Wt-Cap. w/ Nylon Seat w/ Seat Extension FDA UDI

Identifiers

Catalog Number: WCK320AHFAELR FDA UDI
Primary DI / UDI-DI: 05060488573798 FDA UDI
FDA Product Code: IOR FDA UDI
GMDN Term: Push-rim manual 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Height — 37 Inch FDA UDI
Length — 33 Inch FDA UDI
Width — 13 Inch FDA UDI

Category: Push-rim manual wheelchair, non-bariatric

Chariot III by Proactive Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Push-rim manual wheelchair, non-bariatric.

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DRIVEMEDICAL — Drive Devilbiss Healthcare · Class I
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Proactive Medical Products

Sources (1)

FDA UDI ab68a79a-1577-4f2e-9b74-dd6402e3b74d 36 fields · synced May 29, 2026