FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253039979 · Model: MK06860 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10192253039979
Version / Model
MK06860
Catalog Number
MK06860
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-07
Public Version
1
Public Version Date
2022-09-15
Public Version Status
New
Public Device Record Key
a2f3df4d-d730-4ed6-9d87-c7ba2fff463c

Device Description

Kendall™ Holter/Telemetry Kit 9V Battery, 5 Electrodes, Prep Pad, and Single Strap Pouch

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 50192253039977
Primary 10192253039979