Duns Number:187129135
Device Description: Disposable Dissector, angled
Catalog Number
-
Brand Name
Epix ® Inline Laparoscopic Dissector, Angled
Version/Model Number
CY040
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 24, 2016
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
GEI
Product Code Name
Electrosurgical, Cutting & Coagulation & Accessories
Public Device Record Key
bb578808-ca54-40ed-9745-5c4dc7a6491c
Public Version Date
February 10, 2020
Public Version Number
4
DI Record Publish Date
September 24, 2016
Package DI Number
10607915124509
Quantity per Package
10
Contains DI Package
00607915124502
Package Discontinue Date
September 24, 2016
Package Status
Not in Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 499 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 698 |
| 3 | A medical device with high risk that requires premarket approval | 1 |