Catalog Number

9520

Brand Name

Q2 Multiport Extension Set

Version/Model Number

9520

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

ed79f673-9ec6-42cc-9fd0-b78151cb34b4

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 07, 2016

Package DI Number

20634624952007

Quantity per Package

50

Contains DI Package

00634624952003

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper