Duns Number:058614483
Device Description: Monofilament Polypropylene
Catalog Number
-
Brand Name
Surgipro II
Version/Model Number
VP705MX-2
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
K954808,K954808
Product Code
GAW
Product Code Name
Suture, nonabsorbable, synthetic, polypropylene
Public Device Record Key
67318dc6-8933-4d43-b39e-3e3a8703e030
Public Version Date
February 15, 2022
Public Version Number
3
DI Record Publish Date
June 29, 2020
Package DI Number
20884521758428
Quantity per Package
12
Contains DI Package
10884521758421
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |