Catalog Number

-

Brand Name

Polypectomy Snare

Version/Model Number

MD-E-SNC241024

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FGX

Product Code Name

Snare, Non-Electrical

Public Device Record Key

891de1e2-7cbc-494d-a16c-000c64ebff62

Public Version Date

July 18, 2022

Public Version Number

2

DI Record Publish Date

August 26, 2021

Package DI Number

16936534300006

Quantity per Package

10

Contains DI Package

06936534300009

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box