FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kendall

DI: 20192253016700 · Model: 22733 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
3

Basic Information

Brand Name
Kendall
Primary DI
20192253016700
Version / Model
22733
Catalog Number
22733
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2020-11-20
Public Version
2
Public Version Date
2023-06-29
Public Version Status
Update
Public Device Record Key
8ba2c000-5d28-43ea-a0de-41a0f1cefbf6
Distribution End Date
2022-12-04

Device Description

Kendall 700 series Monitoring Clear Tape 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 50192253016701
Primary 20192253016700
Unit of Use 10192253016703