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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
Operating table patient pressure distribution pad, single-use FDA UDI
Device Name
GEO 80" W/VINYL NYLON CVR 4/CS (P01408) FDA UDI
Model / Reference
GEOMATT FDA UDI
Description
GEO 80" W/VINYL NYLON CVR 4/CS (P01408) FDA UDI

Identifiers

Catalog Number
50960-459 FDA UDI
Primary DI / UDI-DI
H93350960459 FDA UDI
FDA Product Code
IKY FDA UDI
GMDN Term
Operating table patient pressure distribution pad, single-use 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating table patient pressure distribution pad, single-use

A comprehensive medical device directory listing Span-America, a single-use operating table patient pressure distribution pad designed to prevent pressure sores and tissue necrosis on prominent parts of the body during extended periods of immobilization.

Similar devices

Also classified as Operating table patient pressure distribution pad, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ffeb86e9-455b-4133-870f-7f846b206cd6 34 fields · synced Jul 21, 2026