FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 20192253016823 · Model: 22935 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Kendall
Primary DI
20192253016823
Version / Model
22935
Catalog Number
22935
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-11-19
Public Version
1
Public Version Date
2020-11-27
Public Version Status
New
Public Device Record Key
cec9b2c3-b12b-4ea6-b457-1e22ebba1cff

Device Description

Kendall Radiolucent Foam Monitoring electrode Tear drop shape

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
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 50192253016824
Primary 20192253016823
Unit of Use 10192253016826