Duns Number:081277700
Device Description: Biopsy Punch, Serrated Lower Jaw, Monopolar HF Port, Single Action, Non-Ratchet Handle wit Biopsy Punch, Serrated Lower Jaw, Monopolar HF Port, Single Action, Non-Ratchet Handle with Rotation Lock
Catalog Number
-
Brand Name
Integra® Miltex®
Version/Model Number
35-401
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 20, 2017
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
K043013
Product Code
HET
Product Code Name
LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
Public Device Record Key
67bc9423-97a6-4f6b-bc12-8d6454a35807
Public Version Date
February 05, 2020
Public Version Number
4
DI Record Publish Date
August 03, 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 |