Duns Number:058614483
Device Description: Bladeless Optical Trocar with Fixation Cannula
Catalog Number
-
Brand Name
Versaport
Version/Model Number
ONB5STF
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"
-
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
K112349,K112349
Product Code
GCJ
Product Code Name
Laparoscope, general & plastic surgery
Public Device Record Key
751576c1-05d6-42fc-a933-18a61d0fd1e0
Public Version Date
February 18, 2022
Public Version Number
6
DI Record Publish Date
September 24, 2016
Package DI Number
20884521134239
Quantity per Package
6
Contains DI Package
10884521134232
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 | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |