← Back to catalogue

Convaid

FDA UDI

Class I (US FDA UDI)

by Convaid Products LLC

Identity

Trade Name
Convaid FDA UDI
Generic Name
Attendant-only-propelled wheelchair, non-bariatric FDA UDI
Model / Reference
TR-14 Trekker Base Standard FDA UDI

Identifiers

Catalog Number
904661 FDA UDI
Primary DI / UDI-DI
10840117404882 FDA UDI
510(k) Number
K140416 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Attendant-only-propelled 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

Yes

FDA UDI

Category: Attendant-only-propelled wheelchair, non-bariatric

Convaid by Convaid Products LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Attendant-only-propelled wheelchair, non-bariatric.

Cleared under the same submission

K140416 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Convaid Products LLC

Sources (1)

  • FDA UDI 145670a3-92d3-4c22-99f3-d835d8a8ff2d 34 fields · synced Jun 9, 2026