FDA UDI In Commercial Distribution 🇺🇸 United States

Composite Kit

DI: 00709078003011 · Model: 0792 · WESTMED, INC.
Product Codes
3
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Composite Kit
Primary DI
00709078003011
Version / Model
0792
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-26
Public Version
4
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
e6476fad-7507-4822-b41c-2412df8baebc

Device Description

Composite Kit, High Flow Humidifier, Adult Cannula, 7' Tubing

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
OGL Oxygen Administration Kit
KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
CAT Cannula, Nasal, Oxygen

GMDN Terms

Code Name
35201 Nasal oxygen cannula, basic
35113 Non-heated respiratory humidifier
60856 Oxygen administration kit

Identifiers

Type ID
Primary 00709078003011