Duns Number:081277700
Device Description: Biopsy Forceps, 9-1/2" Working Length, Roto-Lok™, Monopolar, Double Action, Insulated, 3.5 Biopsy Forceps, 9-1/2" Working Length, Roto-Lok™, Monopolar, Double Action, Insulated, 3.5mm Diameter
Catalog Number
630-178
Brand Name
Integra® Jarit®
Version/Model Number
630178
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
-
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
KNF
Product Code Name
COAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES)
Public Device Record Key
4c9deceb-c866-4ed2-83c5-37dc36fe0a87
Public Version Date
August 01, 2022
Public Version Number
7
DI Record Publish Date
August 24, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 15051 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4286 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 3 |