Duns Number:966390890
Device Description: FreeStyle Libre Pro Reader Kit
Catalog Number
71687
Brand Name
FreeStyle Libre Pro
Version/Model Number
71687
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P150021,P150021
Product Code
MDS
Product Code Name
Sensor, glucose, invasive
Public Device Record Key
4a4f6acc-c89c-4bba-b267-134c85aac2cc
Public Version Date
June 10, 2022
Public Version Number
5
DI Record Publish Date
October 20, 2016
Package DI Number
30357599716876
Quantity per Package
4
Contains DI Package
00357599716875
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 | 13 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 19 |
| 3 | A medical device with high risk that requires premarket approval | 2 |