Catalog Number

-

Brand Name

PDM

Version/Model Number

D332

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

-

Product Code

NEW

Product Code Name

Suture, Surgical, Absorbable, Polydioxanone

Public Device Record Key

74d32db8-7ed3-467c-b545-aee5c8563ffe

Public Version Date

October 17, 2022

Public Version Number

7

DI Record Publish Date

October 16, 2015

Package DI Number

10812444020943

Quantity per Package

12

Contains DI Package

00812444020946

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-