← Back to catalogue

PressureGuard

FDA UDI

Class II (US FDA UDI)

by Span-America Medical Systems, Inc.

Identity

Trade Name
PressureGuard FDA UDI
Generic Name
Alternating-pressure inflator FDA UDI
Device Name
Alternating Pressure Mattress Control Unit FDA UDI
Model / Reference
Easy Air LR FDA UDI
Description
Alternating Pressure Mattress Control Unit FDA UDI

Identifiers

Catalog Number
89667 FDA UDI
Primary DI / UDI-DI
H93389667 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure inflator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 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

No

FDA UDI

Category: Alternating-pressure inflator

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 inflator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ce46208e-85d5-48ed-9c17-a8ad359c982c 34 fields · synced Jun 12, 2026