Dmi

FDA UDI

Class I (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name: DMI FDA UDI
Generic Name: Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name: WHEELCHAIR 18 FIXED FULL ARM- FDA UDI
Model / Reference: 503-0658-0200 FDA UDI
Description: WHEELCHAIR 18 FIXED FULL ARM- FDA UDI

Identifiers

Primary DI / UDI-DI: 00041298006589 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Push-rim manual wheelchair, non-bariatric

Dmi by Dms Holdings, Inc., — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
Probasics — COMPASS HEALTH BRANDS CORP. · Class I
DALTON WIDE MANUAL WHEELCHAIR — Dalton Medical Corp. · Class I
DRIVEMEDICAL — Drive Devilbiss Healthcare · Class I
DRIVEMEDICAL — Drive Devilbiss Healthcare · Class I
Probasics — COMPASS HEALTH BRANDS CORP. · Class I
RoughRider — ROUGHRIDER AMERICA LLC · Class I
JUDITTA — ORMESA SRL · Class I

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: Dms Holdings, Inc.,

Sources (1)

FDA UDI 4925cb42-9a62-4f1d-8e7c-6d9190423b5a 33 fields · synced Jun 1, 2026