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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
Stretcher mattress FDA UDI
Device Name
GM ULTRAMAX STRETCHER 4X26 5 13"HD FDA UDI
Model / Reference
GEOMATTRESS FDA UDI
Description
GM ULTRAMAX STRETCHER 4X26 5 13"HD FDA UDI

Identifiers

Catalog Number
49297BF FDA UDI
Primary DI / UDI-DI
H93349297BF0 FDA UDI
FDA Product Code
IKY FDA UDI
GMDN Term
Stretcher mattress 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: Stretcher mattress

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 Stretcher mattress.

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 4af54ea9-f458-4134-8478-182640f10d4a 34 fields · synced Jun 12, 2026