FDA UDI In Commercial Distribution 🇺🇸 United States

Responsive Respiratory

DI: 00851440007704 · Model: 220-3575 · RESPONSIVE RESPIRATORY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Responsive Respiratory
Primary DI
00851440007704
Version / Model
220-3575
Company Name
RESPONSIVE RESPIRATORY, INC.
Labeler DUNS
129132747
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2024-08-01
Public Version
1
Public Version Date
2024-08-09
Public Version Status
New
Public Device Record Key
3318f5f1-967c-4220-980c-15652d48c864

Device Description

Humidifier Bottle, 6 PSI Safety

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
Yes
Has Expiration Date
Yes
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
Unit of Use 10851440007701
Primary 00851440007704