Catalog Number

-

Brand Name

NAMIC

Version/Model Number

81300021

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

d57302b4-7fd0-4fd1-923a-0165b5804b0e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 17, 2015

Package DI Number

H965813000211

Quantity per Package

100

Contains DI Package

H965813000210

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX