FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884521170568 · Model: 22900 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Kendall
Primary DI
10884521170568
Version / Model
22900
Catalog Number
22900
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
8
Public Version Date
2023-07-03
Public Version Status
Update
Public Device Record Key
dc7047f2-4f2b-4479-8e79-7e41bc45e99a
Distribution End Date
2023-07-01

Device Description

900 Foam Electrodes,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 20884521170565
Primary 10884521170568
Unit of Use 30884521170562

Storage Conditions

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