Catalog Number

TMI1192

Brand Name

NA

Version/Model Number

IUI Catheter, 15cm

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

MQF

Product Code Name

Catheter, Assisted Reproduction

Public Device Record Key

8660628c-0bd5-4c8b-b750-65a503faa072

Public Version Date

January 23, 2019

Public Version Number

3

DI Record Publish Date

October 06, 2016

Package DI Number

10852073002927

Quantity per Package

25

Contains DI Package

00852073002920

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box