Catalog Number

-

Brand Name

Endoplus

Version/Model Number

E311MR-45

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

-

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

K925114

Product Code

HFI

Product Code Name

Coagulator, Culdoscopic (And Accessories)

Public Device Record Key

7027763b-1267-492f-a8fa-768334b1f0fa

Public Version Date

August 21, 2019

Public Version Number

4

DI Record Publish Date

November 08, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-