FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253020977 · Model: 50000095 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10192253020977
Version / Model
50000095
Catalog Number
50000095
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-30
Public Version
2
Public Version Date
2021-08-06
Public Version Status
Update
Public Device Record Key
b6ce0579-7d4e-4b05-94e2-c09083598d94

Device Description

Kendall Fetal Spiral Electrode Attachment Pad

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
No
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
HGP Electrode, circular (spiral), scalp and applicator

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 50192253020975
Primary 10192253020977