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Airlife

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
Airlife FDA UDI
Generic Name
Intravenous/irrigation solution storage container, single-use FDA UDI
Device Name
Airlife™ Modudose™ Sterile Water for Inhalation, USP 5 ml FDA UDI
Model / Reference
AL7025 FDA UDI
Description
Airlife™ Modudose™ Sterile Water for Inhalation, USP 5 ml FDA UDI

Identifiers

Catalog Number
AL7025 FDA UDI
Primary DI / UDI-DI
10889483596081 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Intravenous/irrigation solution storage container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous/irrigation solution storage container, single-use

Airlife by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous/irrigation solution storage container, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI d09cb356-914f-43c9-a5b1-d4d942bebdf3 36 fields · synced May 31, 2026