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Ever-Soft Foam Cushion

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Ever-Soft Foam Cushion FDA UDI
Generic Name
Foam-filled chair cushion FDA UDI
Device Name
Ever-Soft Foam Cushion 18"x18"x2" FDA UDI
Model / Reference
10642 FDA UDI
Description
Ever-Soft Foam Cushion 18"x18"x2" FDA UDI

Identifiers

Primary DI / UDI-DI
00616784064215 FDA UDI
FDA Product Code
IMP FDA UDI
GMDN Term
Foam-filled chair cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Foam-filled chair cushion

Ever-Soft Foam Cushion by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foam-filled chair cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 5d8c9683-049f-4b90-883d-f4ea15af3df5 33 fields · synced Jun 8, 2026