Duns Number:044606982
Device Description: Endopath Blunt Tip Obturator and Housing Assemblies and Adjustable Plugs for the Endopath Endopath Blunt Tip Obturator and Housing Assemblies and Adjustable Plugs for the Endopath Resposable Trocar System
Catalog Number
512BA
Brand Name
ENDOPATH
Version/Model Number
512BA
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 02, 2020
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
GCJ
Product Code Name
Laparoscope, general & plastic surgery
Public Device Record Key
85ec884f-b3cb-486f-9dd1-5b43be1eafdd
Public Version Date
November 03, 2020
Public Version Number
5
DI Record Publish Date
July 15, 2016
Package DI Number
40705036012192
Quantity per Package
36
Contains DI Package
20705036012198
Package Discontinue Date
November 02, 2020
Package Status
Not 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 | 6 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 27 |
| U | Unclassified | 6 |