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PressureGuard

FDA UDI

Class II (US FDA UDI)

by Span-America Medical Systems, Inc.

Identity

Trade Name
PressureGuard FDA UDI
Generic Name
Alternating-pressure bed mattress system FDA UDI
Device Name
Alternating Pressure Mattress FDA UDI
Model / Reference
Advantage Air FDA UDI
Description
Alternating Pressure Mattress FDA UDI

Identifiers

Catalog Number
LM8035AA FDA UDI
Primary DI / UDI-DI
H933LM8035AA0 FDA UDI
FDA Product Code
IOQ FDA UDI
GMDN Term
Alternating-pressure bed mattress system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5170 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: Alternating-pressure bed mattress system

PressureGuard by Span-America Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aba1d0c8-7955-4094-a634-f93250467ef6 34 fields · synced Jun 12, 2026