Duns Number:033029433
Device Description: Forcep case for up to 16 arthroscopic and or sinus forceps interlacing 8 forceps in one di Forcep case for up to 16 arthroscopic and or sinus forceps interlacing 8 forceps in one direction and eight in the other direction, ext size: 9"x15"x5", int size: 8.59"x13.84"x4.84"
Catalog Number
-
Brand Name
Novo Surgical
Version/Model Number
2000-100-025
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
KCT
Product Code Name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Public Device Record Key
5204f0c5-3613-4dac-bacd-6ab74f56f4fc
Public Version Date
July 08, 2021
Public Version Number
3
DI Record Publish Date
May 06, 2019
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 | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2724 |