Catalog Number

KIT-080-00

Brand Name

Micro-Introducer Kit

Version/Model Number

KIT-080-00

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"

Yes

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

OFL

Product Code Name

Percutaneous Sheath Introducer Kit

Public Device Record Key

0fc03c7e-80fa-4207-bae6-7742b14a96bc

Public Version Date

June 07, 2019

Public Version Number

2

DI Record Publish Date

May 23, 2018

Package DI Number

20841268107803

Quantity per Package

100

Contains DI Package

10841268107806

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper Box