FDA UDI In Commercial Distribution 🇺🇸 United States

Honeywell

DI: 00092926207502 · Model: HCM-750 · KAZ USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Honeywell
Primary DI
00092926207502
Version / Model
HCM-750
Company Name
KAZ USA, INC.
Labeler DUNS
122612547
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-31
Public Version
2
Public Version Date
2020-05-27
Public Version Status
Update
Public Device Record Key
fce46bb1-d55c-4ae3-a299-d2af6da64f3f

Device Description

HUMIDIFIER, COOL MOISTURE, EASY CARE, FOR LARGE ROOMS, HONEYWELL

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 70092926207501
Primary 00092926207502

Customer Contacts

Phone
800-477-0457