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American National

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
American National FDA UDI
Generic Name
Alternating-pressure inflator FDA UDI
Device Name
GENESIS III PUMP FOR FDA UDI
Model / Reference
APM-AN-8000-G-PUMP FDA UDI
Description
GENESIS III PUMP FOR FDA UDI

Identifiers

Primary DI / UDI-DI
00092237618110 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

Yes

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

American National by Compass Health Brands Corp. — 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

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Manufacturer

Sources (1)

  • FDA UDI 43c5aa32-99d7-4198-9490-13bb27b7deab 34 fields · synced Jun 6, 2026