Home GUDID 10328785002352 HONEYWELL
Primary DI 10328785002352
Brand HONEYWELL
Company KAZ, INC.
Model HUL900B
Device description HONEYWELL FLAGSHIP ULTRASONIC HUMIDIFIER
Published 2021-09-30
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC true
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 10328785002352 Package GS1 2 In Commercial Distribution 20328785002359 Package GS1 1 In Commercial Distribution 00328785002355 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 10328785002352 10328785002352 20328785002359 20328785002359 00328785002355 00328785002355 328785002355 0328785002355
GMDN Terms# Term, Definition table Term Definition Room humidifier A mains electricity (AC-powered) device intended to add moisture to ambient air, typically to prevent dryness of a patient's airways. This is a stationary device designed to be placed in one location in a room, typically in a hospital, institution, home, or office environment; it can be physically lifted and moved to another position or room. It typically consists of an electric motor, a reservoir for water, an atomizer to produce large mist particles, and a flow diverter. The water reservoir is periodically topped up with clean (preferably purified) water. Moisture is released directly into the room's atmosphere.
Regulatory Flags# DUNS number 001483890 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch false 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 false 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
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