Catalog Number

AST

Brand Name

TROCARTROCAR

Version/Model Number

AST

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"

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

DRC

Product Code Name

Trocar

Public Device Record Key

8d67f967-da37-4035-9c42-c8dc9dbbe66f

Public Version Date

July 15, 2022

Public Version Number

3

DI Record Publish Date

June 29, 2018

Package DI Number

50884908004491

Quantity per Package

5

Contains DI Package

00884908004496

Package Discontinue Date

January 29, 2021

Package Status

Not in Commercial Distribution

Package Type

box