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Span-America

FDA UDI

Class I (US FDA UDI)

by Span-America Medical Systems, Inc.

Identity

Trade Name
Span-America FDA UDI
Generic Name
Foam-filled chair cushion FDA UDI
Device Name
SHORT WAVE SEAT/BACK 20" 4/CS FDA UDI
Model / Reference
SHORT WAVE FDA UDI
Description
SHORT WAVE SEAT/BACK 20" 4/CS FDA UDI

Identifiers

Catalog Number
SWAVE20-04 FDA UDI
Primary DI / UDI-DI
H933SWAVE2004 FDA UDI
FDA Product Code
KIC FDA UDI
GMDN Term
Foam-filled chair cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3175 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

Yes

FDA UDI

Category: Foam-filled chair cushion

Span-America by Span-America Medical Systems, Inc. — 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
Span-America Medical Systems, Inc.

Sources (1)

  • FDA UDI 79f9b18e-08b5-4d26-ae4f-07f399e8aa7f 34 fields · synced Jun 12, 2026