FDA UDI In Commercial Distribution 🇺🇸 United States

KENTEK BLUE SONIC

DI: 00810003754264 · Model: KBS22 · KENTRON HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
KENTEK BLUE SONIC
Primary DI
00810003754264
Version / Model
KBS22
Company Name
KENTRON HEALTHCARE, INC.
Labeler DUNS
618825723
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-18
Public Version
1
Public Version Date
2024-02-26
Public Version Status
New
Public Device Record Key
26fce741-62f0-49ec-92be-1a375af9bc1e

Device Description

KENTEK BLUE SONIC WET GEL EKG ELECTRODES

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No
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 00810003754271
Primary 00810003754264
Package 00810003754288