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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
Low-air-loss bed FDA UDI
Device Name
THE TOPPER REPLACEABLE ZIP OFF OUTER LAYER 84 X 42 FDA UDI
Model / Reference
The Topper FDA UDI
Description
THE TOPPER REPLACEABLE ZIP OFF OUTER LAYER 84 X 42 FDA UDI

Identifiers

Catalog Number
R-MEM8442 FDA UDI
Primary DI / UDI-DI
H933RMEM8442 FDA UDI
FDA Product Code
IKY FDA UDI
GMDN Term
Low-air-loss bed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5150 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Low-air-loss bed

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 Low-air-loss bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cdf03171-cc13-46e1-9ee1-70dc615ebb1a 34 fields · synced Jun 12, 2026