Duns Number:002348191
Device Description: 2.9 MILLIMETER PERCUTANEOUS SHAFT
Catalog Number
PCVSH3
Brand Name
PERCUVANCE
Version/Model Number
IPN055393
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 15, 2021
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
04d14f6e-e72f-44c8-b6f8-ec8220a50916
Public Version Date
June 16, 2021
Public Version Number
4
DI Record Publish Date
July 01, 2019
Package DI Number
34026704667551
Quantity per Package
12
Contains DI Package
24026704667554
Package Discontinue Date
June 15, 2021
Package Status
Not in Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |