← Back to catalogue

AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Non-heated respiratory humidifier FDA UDI
Device Name
AirLife™ Isothermal™ Breathing Circuit Adult Respiratory Circuit MR850 Heated FDA UDI
Model / Reference
RC6Y023034 FDA UDI
Description
AirLife™ Isothermal™ Breathing Circuit Adult Respiratory Circuit MR850 Heated FDA UDI

Identifiers

Catalog Number
RC6Y023034 FDA UDI
Primary DI / UDI-DI
10889483617007 FDA UDI
510(k) Number
K170378 FDA UDI
FDA Product Code
BZE FDA UDI
GMDN Term
Non-heated respiratory humidifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5270 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

Category: Non-heated respiratory humidifier

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

Similar devices

Also classified as Non-heated respiratory humidifier.

Cleared under the same submission

K170378 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI d3e60207-c2c6-4caf-a791-30f7035dd43f 36 fields · synced May 30, 2026