Catalog Number

-

Brand Name

Rotatable Snares

Version/Model Number

MD-E-SNR242524

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

K172758

Product Code

FDI

Product Code Name

Snare, Flexible

Public Device Record Key

52db1ffe-4b51-4203-b375-ff5a96ea14fb

Public Version Date

July 18, 2022

Public Version Number

2

DI Record Publish Date

January 07, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-