FDA UDI In Commercial Distribution 🇺🇸 United States

Resp-O2 Dry Bubble Humidifier

DI: 00840117308855 · Model: 34221 · DYNAREX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Resp-O2 Dry Bubble Humidifier
Primary DI
00840117308855
Version / Model
34221
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-11
Public Version
1
Public Version Date
2022-05-19
Public Version Status
New
Public Device Record Key
7e0816c6-3ecd-4088-8042-75d564fda01d

Device Description

Resp-O2 Dry Bubble Humidifier, 400 mL, 6 PSI (Home Use)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
35113 Non-heated respiratory humidifier

Identifiers

Type ID
Primary 00840117308855
Package 00840117308862