Duns Number:017524666
Device Description: Premium UNIFY PDO Sutures, Sm 5-0, 13mm 3/8 circle Rev Cut, 18"
Catalog Number
-
Brand Name
Premium UNIFY PDO Sutures
Version/Model Number
PSD-518R13
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K022666,K073614,K173779,K022666,K073614,K173779,K022666,K073614,K173779
Product Code
NEW
Product Code Name
Suture, Surgical, Absorbable, Polydioxanone
Public Device Record Key
c114af1a-22c8-4437-b934-725ee56f708a
Public Version Date
February 05, 2021
Public Version Number
7
DI Record Publish Date
November 04, 2016
Package DI Number
20814639022708
Quantity per Package
100
Contains DI Package
10814639022701
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 | 73 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 121 |