FDA UDI In Commercial Distribution 🇺🇸 United States

OxyGo Bubble Humidifier

DI: 00709078005954 · Model: 1425-1014 · WESTMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
OxyGo Bubble Humidifier
Primary DI
00709078005954
Version / Model
1425-1014
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-25
Public Version
1
Public Version Date
2018-10-26
Public Version Status
New
Public Device Record Key
8b3b3ba0-569e-41ff-97fb-9bca4ba648c5

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 10709078005951
Primary 00709078005954