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Motion composites

FDA UDI

Class I (US FDA UDI)

by Motion Composites

Identity

Trade Name
Motion composites FDA UDI
Generic Name
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible FDA UDI
Device Name
wheelchair mechanical FDA UDI
Model / Reference
Helio A7 FDA UDI
Description
wheelchair mechanical FDA UDI

Identifiers

Primary DI / UDI-DI
00811774000017 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible

Motion composites by Motion Composites — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Motion Composites

Sources (1)

  • FDA UDI a99b1dfd-22ab-4dc4-a843-7f4560e99d9b 35 fields · synced May 30, 2026