Catalog Number

-

Brand Name

Polypectomy Snare

Version/Model Number

MD-E-SNC241518

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

472f9e06-58d1-42b3-98f8-90e85f22029d

Public Version Date

July 18, 2022

Public Version Number

2

DI Record Publish Date

May 10, 2021

Package DI Number

16974173020015

Quantity per Package

10

Contains DI Package

06974173020797

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box