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Litestream XF

FDA UDI

Class I (US FDA UDI)

by Pride Mobility Products Corp.

Identity

Trade Name
Litestream XF FDA UDI
Generic Name
Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name
A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA UDI
Model / Reference
Litestream XF/Litestream Hemi/Litestream HD FDA UDI
Description
A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00606509600019 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

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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Push-rim manual wheelchair, non-bariatric

Litestream XF by Pride Mobility Products Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d5a271fa-5449-4a6c-a6b3-cf15a8d1a5d8 34 fields · synced Jun 4, 2026