FDA UDI In Commercial Distribution 🇺🇸 United States

Vicks

DI: 00328785039009 · Model: V3900 · KAZ USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vicks
Primary DI
00328785039009
Version / Model
V3900
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
e083150c-1b4a-4bc5-8981-e69e4dc0c142

Device Description

HUMIDIFIER, COOLMIST, GERM FREE, VICKS, 1PC MASTER

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 10328785039006
Primary 00328785039009

Customer Contacts

Phone
800-477-0547