Catalog Number

ECN-E12048L

Brand Name

POLYESTER

Version/Model Number

ECN-E12048L

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

GAT

Product Code Name

Suture, Nonabsorbable, Synthetic, Polyethylene

Public Device Record Key

18168b6c-9cdf-442b-a331-b2a824f3eb5f

Public Version Date

February 05, 2021

Public Version Number

6

DI Record Publish Date

June 20, 2016

Package DI Number

20790986006465

Quantity per Package

12

Contains DI Package

10790986006536

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-