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AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Inhalation therapy saline solution, isotonic FDA UDI
Device Name
SODIUM CHLORIDE SOLUTION 0.45% 1000mL FDA UDI
Model / Reference
CN4510 FDA UDI
Description
SODIUM CHLORIDE SOLUTION 0.45% 1000mL FDA UDI

Identifiers

Catalog Number
CN4510 FDA UDI
Primary DI / UDI-DI
10889483598665 FDA UDI
510(k) Number
K830895 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Inhalation therapy saline solution, isotonic 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inhalation therapy saline solution, isotonic

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

Similar devices

Also classified as Inhalation therapy saline solution, isotonic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 7d14b181-e420-4545-b301-9628880e4fbf 36 fields · synced May 30, 2026