FDA UDI In Commercial Distribution 🇺🇸 United States

Vicks

DI: 00328785037005 · Model: V3700 · KAZ USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Vicks
Primary DI
00328785037005
Version / Model
V3700
Company Name
KAZ USA, INC.
Labeler DUNS
122612547
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-30
Public Version
2
Public Version Date
2020-05-27
Public Version Status
Update
Public Device Record Key
a6561842-de9e-42e3-90b8-e091e9b19597

Device Description

HUMIDIFIER, COOL MOISTURE, STARRY NIGHT, VICKS

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 70328785037004
Primary 00328785037005
Package 10328785037002

Customer Contacts

Phone
800-477-0457