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Ease Cushion

FDA UDI

Class II (US FDA UDI)

by Ease Seating Systems

Identity

Trade Name
Ease Cushion FDA UDI
Generic Name
Alternating-pressure chair cushion, reusable FDA UDI
Device Name
20" x 18" cushion FDA UDI
Model / Reference
20x18 Cushion FDA UDI
Description
20" x 18" cushion FDA UDI

Identifiers

Primary DI / UDI-DI
00860000915397 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure chair cushion, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 FDA UDI
Commercial Distribution
Not 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Ease Cushion by Ease Seating Systems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6007aecf-94bc-4fa7-8a62-a5dd87acf4c3 35 fields · synced May 30, 2026