Home GUDID 00840117308855 Resp-O2 Dry Bubble Humidifier, 6 PSI (Home Use), 400 mL
Primary DI 00840117308855
Brand Resp-O2 Dry Bubble Humidifier, 6 PSI (Home Use), 400 mL
Company Dynarex Corporation
Model 34221
Published 2022-05-11
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
Single use false 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 00840117308862 Package GS1 50 In Commercial Distribution 00840117308855 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 00840117308862 00840117308862 840117308862 0840117308862 00840117308855 00840117308855 840117308855 0840117308855
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 008124539 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# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00840117341913 Steel Button Folding Walker, Adult, With 5" Wheel, 32" - 39" 10170-4 2026-08-03 00840117338067 Resp-O2 M24 Oxygen E-Cylinder With CGA 870 Toggle Valve, 4.55 L 36390-T 2024-07-25 00840117338135 Resp-O2 M15 Oxygen Standard D-Cylinder 2.89 L, With CGA 870 Post Valve 36394 2024-07-25 00840117326156 Resp-O2 M9 Oxygen C-Cylinder 1.7L 36392 2023-12-29 00840117327511 Resp-O2 M6 Oxygen B-Cylinder,1L With CGA870 Post Valve 36393 2023-12-29 00840117327528 Resp-O2 M15 Oxygen D-Cylinder, 2.9 L With CGA 870 Post Valve 36391 2023-12-29 00840117326125 Resp-O2 M24 Oxygen E-Cylinder, With CGA870 Post Valve 36390 2023-03-24 00840117310162 Resp-O2 Fingertip Pulse Oximeter, For Adult Use 36400 2021-12-22 00840117341241 Aluminum Crutches, Child, 4'0" - 4'6" 10100-8 2026-07-31 00840117341258 Aluminum Crutches, Youth, 4'6" - 5'2" 10101-8 2026-07-31 00840117341265 Aluminum Crutches, Adult, 5'2" - 5'10" 10102-8 2026-07-31 00840117341272 Aluminum Crutches, Tall, 5'10" - 6'6" 10103-8 2026-07-31 00840117341357 Forearm Crutches, Youth, 4'2" - 5'2" 10110-6 2026-07-31 00840117341364 Forearm Crutches, Adult, 5'0" - 6'2" 10111-6 2026-07-31 00840117341371 Forearm Crutches, Tall, 5'10" - 6'6" 10112-6 2026-07-31 00840117346253 Pill Crusher Pouches with Round Corners 4210R 2026-07-31 00840117349551 Drape Sheets, Polypropylene/Polyethylene 2-ply, Black, 40" x 90" (101.6 cm x 228 8156 2026-07-31 00840117350069 Pillow Cases, Polypropylene/Polyethylene 2-ply, Black, 21" x 30" 8167 2026-07-31 00840117351684 Universal Catheterization Procedure Trays with 2000 mL Anti-Reflux Drainage Bag 5003 2026-07-31 00840117351875 Resp-O2 Single Suction Catheters, Pediatric Graduated Catheter 32000S 2026-07-31
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 06971156891849 Equate WAL-MART STORES, INC. KFZ 2026-07-31 04719874957315 Create Biotech CREATE BIOTECH CO., LTD. KFZ 2026-07-21 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 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