← Back to catalogue

AirFloat Static Air Seat Cushion

FDA UDI

Class I (US FDA UDI)

by Primo Inc

Identity

Trade Name
AirFloat Static Air Seat Cushion FDA UDI
Generic Name
Wheelchair seat cushion FDA UDI
Device Name
AirFloat Static Air Seat Cushion (19"x19") with pump FDA UDI
Model / Reference
AF1919P FDA UDI
Description
AirFloat Static Air Seat Cushion (19"x19") with pump FDA UDI

Identifiers

Catalog Number
AF1919P FDA UDI
Primary DI / UDI-DI
00810006684117 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Wheelchair seat cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair seat cushion

AirFloat Static Air Seat Cushion by Primo Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair seat cushion.

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
Primo Inc

Sources (1)

  • FDA UDI 776b477e-4ebc-4603-944e-4e714a5427cc 34 fields · synced May 30, 2026