Catalog Number

-

Brand Name

Multi-Snare

Version/Model Number

147304

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

K011783,K011783,K011783

Product Code

DXE

Product Code Name

Catheter, Embolectomy

Public Device Record Key

ac9d315c-dd52-4b1d-8887-7e9cc74a0992

Public Version Date

July 08, 2021

Public Version Number

4

DI Record Publish Date

May 15, 2017

Package DI Number

00813623011519

Quantity per Package

25

Contains DI Package

04042301061812

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case