Home GUDID 10709078005951 OxyGo Bubble Humidifier
Primary DI 10709078005951
Brand OxyGo Bubble Humidifier
Company WESTMED, INC.
Model 1425-1014
Device description Bubble Humidifier, Dry
Published 2018-09-25
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KFZ Humidifier, Non-Direct Patient Interface (Home-Use) Anesthesiology 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10709078005951 Package GS1 50 In Commercial Distribution 00709078005954 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 10709078005951 10709078005951 00709078005954 00709078005954 709078005954 0709078005954
GMDN Terms# Term, Definition table Term Definition Non-heated respiratory humidifier A device designed to prevent the drying of airway passages associated with the inhalation of oxygen (O2) by adding water vapour to the dry gas as it is passed through, or more seldom, over water. It typically consists of a graduated container (reservoir) for the water, a top piece that functions as a detachable lid (typically a screw lid with a gastight seal), and a tube that protrudes into the water to divert the gas below the water level. This device, commonly known as a bubble humidifier, does not heat the water. It has connectors: 1) one (e.g., a winged nut) that connects to an oxygen therapy flowmeter; and 2) one to which the patient tubing is connected. This is a reusable device.
Regulatory Flags# DUNS number 092673953 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex true Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00194346604845 Equate WAL-MART STORES, INC. KFZ 2026-02-16 00328785008234 HONEYWELL KAZ USA, INC. KFZ 2026-02-04 00328785008258 Honeywell KAZ USA, INC. KFZ 2026-02-04 00328785012828 Vicks KAZ USA, INC. KFZ 2026-02-04 00328785101539 Vicks KAZ USA, INC. KFZ 2026-02-04 00328785002263 Honeywell KAZ USA, INC. KFZ 2026-02-04 10328785008231 HONEYWELL KAZ USA, INC. KFZ 2026-02-04 10328785008255 Honeywell KAZ USA, INC. KFZ 2026-02-04 00328785012804 Vicks KAZ USA, INC. KFZ 2026-02-04 00328785012811 Vicks KAZ USA, INC. KFZ 2026-02-04 10328785012825 Vicks KAZ USA, INC. KFZ 2026-02-04 00328785012835 Vicks KAZ USA, INC. KFZ 2026-02-04 10328785101536 Vicks KAZ USA, INC. KFZ 2026-02-04 00328785008241 HONEYWELL KAZ USA, INC. KFZ 2026-02-03 00050428005583 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED KFZ 2026-01-28 00328785009620 VICKS KAZ USA, INC. KFZ 2026-01-28 00328785013863 Vicks KAZ USA, INC. KFZ 2026-01-28 00328785014426 Vicks KAZ USA, INC. KFZ 2026-01-28 00050428005606 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED KFZ 2026-01-26 10050428005603 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED KFZ 2026-01-26 00050428005613 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED KFZ 2026-01-23 10050428005610 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED KFZ 2026-01-23 10889483054338 AirLife™ SUNMED, LLC KFZ 2025-12-19 10889483229422 AirLife™ SUNMED, LLC KFZ 2025-12-19 20889483054335 AirLife™ SUNMED, LLC KFZ 2025-12-19 20889483229429 AirLife™ SUNMED, LLC KFZ 2025-12-19 10889483054321 AirLife™ SUNMED, LLC KFZ 2025-12-18 00328785002454 Vicks KAZ, INC. KFZ 2025-05-05 00328785002478 Vicks KAZ, INC. KFZ 2025-05-05 00851440007704 Responsive Respiratory RESPONSIVE RESPIRATORY, INC. KFZ 2024-08-01