FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884521186170 · Model: 2293005 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Kendall
Primary DI
10884521186170
Version / Model
2293005
Catalog Number
2293005
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
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
bfdf72a9-49d3-43c8-8bd0-9f6cb46d847c

Device Description

Adult 930 Foam Electrodes,Prewired, 5 Lead, Conductive Adhesive Hydrogel, Radiolucent

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 20884521186177
Primary 10884521186170
Unit of Use 30884521186174

Customer Contacts

Storage Conditions

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