FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884527010349 · Model: MK06860 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10884527010349
Version / Model
MK06860
Catalog Number
MK06860
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2021-05-17
Public Version Status
Update
Public Device Record Key
fc83054e-4b32-4e47-8b84-ac4b321617c7

Device Description

True content to be populated as part of rebranding

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
17460 Neonatal electrocardiographic electrode

Identifiers

Type ID
Package 20884527010346
Primary 10884527010349

Customer Contacts