Duns Number:344007369
Device Description: The LiftUp Kit contains the LiftUp injection solution (5 vials with 20 ml each) and inject The LiftUp Kit contains the LiftUp injection solution (5 vials with 20 ml each) and injection accessories (10 syringes and 5 injection needles).
Catalog Number
200.56.02
Brand Name
LiftUp Kit
Version/Model Number
LiftUp Kit
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"
Yes
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
PLL
Product Code Name
Submucosal Injection Agent
Public Device Record Key
f1efd98d-77c3-46a3-a039-87592fe1ea73
Public Version Date
August 30, 2022
Public Version Number
1
DI Record Publish Date
August 22, 2022
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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 8 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 61 |