Duns Number:063997360
Device Description: LDR Blood Glucose Monitoring System
Catalog Number
5277181
Brand Name
LEADER
Version/Model Number
5277181
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K132086,K132086,K132086,K132086
Product Code
CGA
Product Code Name
Glucose Oxidase, Glucose
Public Device Record Key
76daa468-c29e-4b4f-ade7-a377ef6cf88c
Public Version Date
July 02, 2021
Public Version Number
5
DI Record Publish Date
April 26, 2017
Package DI Number
50096295129149
Quantity per Package
6
Contains DI Package
30096295129145
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 23 |
2 | A medical device with a moderate to high risk that requires special controls. | 39 |