Catalog Number

S-923

Brand Name

DEKNATEL

Version/Model Number

IPN025492

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

GAP

Product Code Name

SUTURE, NONABSORBABLE, SILK

Public Device Record Key

f24fb57c-67dd-44cd-907c-185815b91fd7

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

March 24, 2017

Package DI Number

34026704424321

Quantity per Package

36

Contains DI Package

14026704424327

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box