FDA UDI In Commercial Distribution 🇺🇸 United States

KenTeK

DI: 00810003751171 · Model: KT-2000 · KENTRON HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KenTeK
Primary DI
00810003751171
Version / Model
KT-2000
Catalog Number
KT-2000
Company Name
KENTRON HEALTHCARE, INC.
Labeler DUNS
618825723
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-18
Public Version
3
Public Version Date
2022-12-26
Public Version Status
Update
Public Device Record Key
16d242dd-963d-4ea0-b49e-a8825dd89945

Device Description

KenTeK FINGER PULSE OXIMETER WITH OLED SCREEN, MEASURE BLOOD OXYGEN SATURATION LEVEL AND PULSE RATE, PR WAVEFORM DISPLAY, LOW BATTERY INDICATOR, AUTOMATIC POWER OFF, FOUR DIRECTIONS DISPLAY.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
DQA Oximeter

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Primary 00810003751171

Customer Contacts

Phone
615-384-0573