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Dalton Manual Wheelchair

FDA UDI

Class I (US FDA UDI)

by Dalton Medical Corp.

Identity

Trade Name
DALTON MANUAL WHEELCHAIR FDA UDI
Generic Name
Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name
WHEELCHAIR, MANUAL, 16" W/FOOTREST, WT LIMIT 250 LBS FDA UDI
Model / Reference
K416F0215 FDA UDI
Description
WHEELCHAIR, MANUAL, 16" W/FOOTREST, WT LIMIT 250 LBS FDA UDI

Identifiers

Primary DI / UDI-DI
00815027011096 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

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

Dalton Manual Wheelchair by Dalton Medical 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

Manufacturer
Dalton Medical Corp.

Sources (1)

  • FDA UDI 4f437df3-5dbb-43fb-aad4-c3d3d1b42d63 33 fields · synced May 30, 2026