Catalog Number

-

Brand Name

ENDOGATOR

Version/Model Number

100125F

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 03, 2022

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

-

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

K033695,K033695,K033695

Product Code

OCX

Product Code Name

Endoscopic Irrigation/Suction System

Public Device Record Key

9b1a8b2d-bdd6-4c9b-9136-226f04eaf569

Public Version Date

May 04, 2022

Public Version Number

9

DI Record Publish Date

September 22, 2016

Package DI Number

20677964058435

Quantity per Package

50

Contains DI Package

00677964058431

Package Discontinue Date

May 03, 2022

Package Status

Not in Commercial Distribution

Package Type

Case