Duns Number:044606982
Device Description: Endopath ETS Flex Endoscopic Articulating Linear Cutter
Catalog Number
ATB35
Brand Name
ENDOPATH
Version/Model Number
ATB35
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 06, 2017
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
GDW
Product Code Name
STAPLE, IMPLANTABLE
Public Device Record Key
1073d05e-2031-4b84-8750-f36a980c4bb8
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 24, 2015
Package DI Number
40705036012314
Quantity per Package
9
Contains DI Package
20705036012310
Package Discontinue Date
June 06, 2017
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 |