Duns Number:079402290
Device Description: Blue Monofilament Polypropylene, Nonabsorbable Surgical Suture
Catalog Number
D10195
Brand Name
PROLENE
Version/Model Number
D10195
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
K133356,K133356
Product Code
GAW
Product Code Name
Suture, nonabsorbable, synthetic, polypropylene
Public Device Record Key
e9eaf98f-0f0d-4a6e-88f4-8439db02e99b
Public Version Date
February 05, 2021
Public Version Number
2
DI Record Publish Date
October 01, 2019
Package DI Number
30705031464265
Quantity per Package
12
Contains DI Package
10705031464261
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 |