Catalog Number

MCITX-1

Brand Name

MCI

Version/Model Number

MCITX-1

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

OWL

Product Code Name

Peripheral catheter insertion kit

Public Device Record Key

b984dece-4920-4622-b60d-9da947fca8c7

Public Version Date

June 07, 2019

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

38498840009605

Quantity per Package

20

Contains DI Package

08498840009604

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-