Duns Number:071595540
Device Description: OPTIMIZER Polypectomy Snare; Medium Oval Loop, Firm Wire, Microvasive Connector
Catalog Number
000475
Brand Name
OPTIMIZER
Version/Model Number
000475
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 11, 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
FDI
Product Code Name
SNARE, FLEXIBLE
Public Device Record Key
ca78c110-8e6e-471f-b4a1-9a5d1927dfc2
Public Version Date
April 12, 2022
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
20653405053399
Quantity per Package
10
Contains DI Package
10653405053392
Package Discontinue Date
April 11, 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 |