Duns Number:071595540
Device Description: CONMED FLEXITIP DISPOSABLE SCLEROTHERAPY NEEDLE
Catalog Number
000200
Brand Name
CONMED FLEXITIP
Version/Model Number
000200
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 02, 2022
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
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
GAA
Product Code Name
NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE
Public Device Record Key
3d854875-c342-4506-bdff-68a76429e168
Public Version Date
May 03, 2022
Public Version Number
2
DI Record Publish Date
October 05, 2021
Package DI Number
10653405051213
Quantity per Package
1
Contains DI Package
30653405051217
Package Discontinue Date
May 02, 2022
Package Status
Not in Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1412 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2261 |
| 3 | A medical device with high risk that requires premarket approval | 95 |