FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 20192253017240 · Model: 31078135 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
30

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Basic Information

Brand Name
Kendall
Primary DI
20192253017240
Version / Model
31078135
Catalog Number
31078135
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2024-05-01
Public Version
2
Public Version Date
2026-04-10
Public Version Status
Update
Public Device Record Key
731558c3-379f-43f5-b1c0-3018d7ccea8b

Device Description

Kendall 200 series Foam Monitoring electrode Teardrop 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 50192253017241
Primary 20192253017240
Unit of Use 10192253017243

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
12 – 32 Degrees Celsius