Duns Number:058614483
Device Description: Monofilament Polypropylene
Catalog Number
-
Brand Name
Surgipro II
Version/Model Number
XX-5170
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 03, 2015
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
GAW
Product Code Name
SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
Public Device Record Key
96926ea3-e831-46d7-aeb1-0d05d3bf1595
Public Version Date
August 22, 2022
Public Version Number
5
DI Record Publish Date
September 03, 2015
Package DI Number
20884521137223
Quantity per Package
36
Contains DI Package
10884521137226
Package Discontinue Date
September 03, 2015
Package Status
Not 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 |