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AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Nebulizing adaptor FDA UDI
Device Name
AirLife™ Isothermal Breathing Circuit Accessory Special Product Request - 10mm Nebulizer Adapter FDA UDI
Model / Reference
4220-504 FDA UDI
Description
AirLife™ Isothermal Breathing Circuit Accessory Special Product Request - 10mm Nebulizer Adapter FDA UDI

Identifiers

Catalog Number
4220-504 FDA UDI
Primary DI / UDI-DI
10889483583357 FDA UDI
510(k) Number
K023602 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing adaptor 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI

Category: Nebulizing adaptor

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

Similar devices

Also classified as Nebulizing adaptor.

Cleared under the same submission

K023602 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 66282755-2970-4b05-9a0c-7335d6ba7812 37 fields · synced Jun 8, 2026