FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 30884527004878 · Model: ES82650 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
Kendall
Primary DI
30884527004878
Version / Model
ES82650
Catalog Number
ES82650
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
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
32da0fbc-5e11-4cbb-b84c-68b3a945c466

Device Description

SF450 Foam Electrodes,Conductive Adhesive Hydrogel

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 10884527004874
Primary 30884527004878
Package 20884527004871
Unit of Use 40884527004875

Customer Contacts

Storage Conditions

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