Catalog Number

7210192S

Brand Name

NA

Version/Model Number

7210192S

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 05, 2017

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

-

Product Code

FEI

Product Code Name

INSTRUMENT, SPECIAL LENS, FOR ENDOSCOPE

Public Device Record Key

b88c93a1-c59c-4826-a0fa-fd810d0854e0

Public Version Date

March 19, 2021

Public Version Number

3

DI Record Publish Date

September 28, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-