FDA UDI In Commercial Distribution 🇺🇸 United States

Bubble Humidifier

DI: 00709078007606 · Model: 0480 · WESTMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bubble Humidifier
Primary DI
00709078007606
Version / Model
0480
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-24
Public Version
1
Public Version Date
2021-03-04
Public Version Status
New
Public Device Record Key
5bd8a7e6-a0a0-41a1-a1e7-f3238d67e338

Device Description

Bubble Humidifier, Dry

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
35113 Non-heated respiratory humidifier

Identifiers

Type ID
Package 10709078007603
Primary 00709078007606