Catalog Number

TSIL1863

Brand Name

Transseptal Introducer

Version/Model Number

TSIL1863

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

K181031,K181031

Product Code

DYB

Product Code Name

Introducer, Catheter

Public Device Record Key

ef222998-5341-4859-9929-1ac2aca264dc

Public Version Date

June 07, 2019

Public Version Number

2

DI Record Publish Date

November 09, 2018

Package DI Number

30858769006280

Quantity per Package

5

Contains DI Package

00858769006289

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box