FDA UDI In Commercial Distribution 🇺🇸 United States

CURO L5

DI: 00860394001225 · Model: CURO L5 CURO L5 · KPI HEALTHCARE, INC.
Product Codes
6
GMDN Terms
12
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURO L5
Primary DI
00860394001225
Version / Model
CURO L5 CURO L5
Company Name
KPI HEALTHCARE, INC.
Labeler DUNS
087243403
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-26
Public Version
4
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
032176df-3efc-4201-8480-6a77d8be77cd

Device Description

CURO L5 Cholesterol and Glucose measuring system

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NBW System, Test, Blood Glucose, Over The Counter
CGA Glucose Oxidase, Glucose
CHH Enzymatic Esterase--Oxidase, Cholesterol
JGY Colorimetric Method, Triglycerides
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)
LBR Ldl & Vldl Precipitation, Hdl

GMDN Terms

Code Name
64125 Multiple physiological parameter spot-check system analyser
62792 Glucose/ketone/lipid monitoring system IVD, home-use
62538 Glucose monitoring system IVD, point-of-care
62646 Glucose analyser IVD, point-of-care
56686 Glucose analyser IVD, laboratory, automated/semi-automated
62739 Glucose analyser IVD, laboratory, manual
44206 Glucose analyser IVD, laboratory, automated
62645 Glucose analyser IVD, home-use
63088 Blood glucose/blood pressure monitoring system, point-of-care
62537 Glucose monitoring system IVD, home-use
63087 Blood glucose/blood pressure monitoring system, home-use
60770 Ambulatory insulin infusion pump/interstitial glucose monitoring system

Identifiers

Type ID
Primary 00860394001225

Premarket Submissions

Submission Number Supplement Number
K130295 000