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Medline Industries, Inc.

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name
WHEELCHAIR,RECLINER,EXCEL,22IN,DLA,ELR FDA UDI
Model / Reference
MDS808650 FDA UDI
Description
WHEELCHAIR,RECLINER,EXCEL,22IN,DLA,ELR FDA UDI

Identifiers

Catalog Number
MDS808650 FDA UDI
Primary DI / UDI-DI
00080196303208 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

No

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Push-rim manual wheelchair, non-bariatricWheelchair, power-assisted, occupant-controlled, collapsible

Medline Industries, Inc. by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair, power-assisted, occupant-controlled, collapsible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI a6d735b1-f59e-40c8-89d2-ab9006012148 35 fields · synced May 30, 2026