← Back to catalogue

Wavon

FDA UDI

Class I (US FDA UDI)

by Ease Seating Systems

Identity

Trade Name
Wavon FDA UDI
Generic Name
Alternating-pressure chair cushion, reusable FDA UDI
Device Name
Alternating Pressure Seat Cushion FDA UDI
Model / Reference
Wavon 18x18 FDA UDI
Description
Alternating Pressure Seat Cushion FDA UDI

Identifiers

Primary DI / UDI-DI
00860010877487 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Alternating-pressure chair cushion, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 18 Inch FDA UDI
Width — 18 Inch FDA UDI

Category: Alternating-pressure chair cushion, reusable

Wavon by Ease Seating Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure chair cushion, reusable.

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
Ease Seating Systems

Sources (1)

  • FDA UDI 59aa6fe3-a08b-40e9-967f-6c36a3d4275b 34 fields · synced May 29, 2026