AirLife™

FDA UDI

Class III (US FDA UDI)

by Vyaire Medical, Inc.

Identity

Trade Name: AirLife™ FDA UDI
Generic Name: Desk mount FDA UDI
Device Name: KIT AUTOFEED POLE/BRKT FDA UDI
Model / Reference: 770136 FDA UDI
Description: KIT AUTOFEED POLE/BRKT FDA UDI

Identifiers

Catalog Number: 770136 FDA UDI
Primary DI / UDI-DI: 10190752176744 FDA UDI
PMA Number: P890057 FDA UDI
FDA Product Code: LSZ FDA UDI
GMDN Term: Desk mount FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Desk mount

AirLife™ by Vyaire Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Desk mount.

Equipment Mount — LIFEPORT, LLC. · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
Incubator Attachment Plates — LIFEPORT, LLC. · Class I
Equipment Mount — LIFEPORT, LLC. · Class I
Equipment Mount — LIFEPORT, LLC. · Class I
Equipment Mount — LIFEPORT, LLC. · Class I
AeroSled Utility Deck (TD) — LIFEPORT, LLC. · Class I
Overhead Equipment Rack — LIFEPORT, LLC. · Class I

Cleared under the same submission

P890057 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Vyaire Medical, Inc.

Sources (1)

FDA UDI 740e2c75-8c32-4112-a8d1-50f7fd914573 36 fields · synced May 30, 2026