FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kendall

DI: 20192253017714 · Model: 31177721 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
2

Basic Information

Brand Name
Kendall
Primary DI
20192253017714
Version / Model
31177721
Catalog Number
31177721
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2023-06-15
Public Version
1
Public Version Date
2023-06-23
Public Version Status
New
Public Device Record Key
6e791e5a-b2fa-4c04-884a-a8c77b2c9e09
Distribution End Date
2023-06-15

Device Description

KENDALL 1210H Defibrillation Electrode, Nonsterile, Product Code 31177721

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
No
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
MKJ Automated External Defibrillators (Non-Wearable)

GMDN Terms

Code Name
11130 Electrode conductive skin pad, single-use

Identifiers

Type ID
Package 50192253017715
Primary 20192253017714
Unit of Use 10192253017717

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from Light
Type
Storage Environment Temperature
Temperature Range
15 – 35 Degrees Celsius