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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
Metro 16 FDA UDI

Identifiers

Catalog Number
901335 FDA UDI
Primary DI / UDI-DI
10840117401027 FDA UDI
510(k) Number
K810676 FDA UDI
FDA Product Code
LBE 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

K810676 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Convaid Products LLC

Sources (1)

  • FDA UDI 9d173a6d-8559-42b4-b0f2-dcaf5e48ae94 34 fields · synced Jun 9, 2026