Catalog Number

29-7269M8

Brand Name

DEKNATEL

Version/Model Number

IPN004790

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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"

Yes

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

GAQ

Product Code Name

Suture, nonabsorbable, steel, monofilament and multifilament, sterile

Public Device Record Key

075d1d3f-bfdb-4388-9503-cbbf456069b8

Public Version Date

February 05, 2021

Public Version Number

5

DI Record Publish Date

July 25, 2018

Package DI Number

34026704419532

Quantity per Package

12

Contains DI Package

14026704419538

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box