Duns Number:827900809
Device Description: Assembly, Pump Replacement, Refurbished, t:flex
Catalog Number
-
Brand Name
t:flex Insulin Pump, Replacement, Refurbished
Version/Model Number
007473
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
Yes
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
-
Product Code
LZG
Product Code Name
Pump, Infusion, Insulin
Public Device Record Key
88bcdb27-5ce9-41e3-a262-c7255d8cbd24
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 11, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 35 |
3 | A medical device with high risk that requires premarket approval | 16 |