FDA UDI In Commercial Distribution 🇺🇸 United States

HONEYWELL

DI: 00328785002355 · Model: HUL900B · KAZ, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
HONEYWELL
Primary DI
00328785002355
Version / Model
HUL900B
Company Name
KAZ, INC.
Labeler DUNS
001483890
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-30
Public Version
1
Public Version Date
2021-10-08
Public Version Status
New
Public Device Record Key
ba63809f-ef20-406e-a5fb-c375b1c2e0b0

Device Description

HONEYWELL FLAGSHIP ULTRASONIC HUMIDIFIER

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KFZ Humidifier, Non-Direct Patient Interface (Home-Use)

GMDN Terms

Code Name
16759 Room humidifier

Identifiers

Type ID
Package 10328785002352
Primary 00328785002355
Package 20328785002359

Customer Contacts

Phone
800-477-0457