Duns Number:829465157
Device Description: Blue Monofilament Poly(Hexafluoropropylene-VDF), Nonabsorbable Surgical Suture
Catalog Number
PNM3706
Brand Name
PRONOVA
Version/Model Number
PNM3706
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
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
K001625,K001625
Product Code
GAW
Product Code Name
SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
Public Device Record Key
7c30b2bf-5573-4886-a7b4-35fb89bcf0a3
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
September 28, 2018
Package DI Number
30705031246359
Quantity per Package
12
Contains DI Package
10705031246355
Package Discontinue Date
-
Package Status
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 | 6 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1028 |
| 3 | A medical device with high risk that requires premarket approval | 15 |
| U | Unclassified | 1 |