FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 20192253016977 · Model: 31.1917.21 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
Kendall
Primary DI
20192253016977
Version / Model
31.1917.21
Catalog Number
31.1917.21
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2022-03-08
Public Version
1
Public Version Date
2022-03-16
Public Version Status
New
Public Device Record Key
f5e4d23c-cf7d-482c-9381-a18df98ea7a6

Device Description

Kendall H91SSG Foam Monitoring electrode with Hydrogel ( 57x34mm)

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
MR Unsafe
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
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 50192253016978
Package 30192253016974
Primary 20192253016977
Unit of Use 10192253016970

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius