FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 20884527007889 · Model: 10415041 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
3

Basic Information

Brand Name
Kendall
Primary DI
20884527007889
Version / Model
10415041
Catalog Number
10415041
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2019-02-15
Public Version Status
Update
Public Device Record Key
3c254edf-5607-4688-b4b1-acdcd0ed48a7

Device Description

Wet Gel Electrodes,GC-13 Foam

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 10884527007882
Primary 20884527007889
Package 40884527007883
Unit of Use 50884527007880

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry;AVOID DIRECT SUNLIGHT