Catalog Number

95902

Brand Name

Q2 Extension Set 17 in (43.2 cm)

Version/Model Number

95902

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

-

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

d053add7-5e7d-4fe9-a527-c7b9bd0c81b9

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 29, 2016

Package DI Number

20634624959020

Quantity per Package

100

Contains DI Package

00634624959026

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper