Catalog Number

-

Brand Name

Portex

Version/Model Number

4903

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

K952516,K952516

Product Code

JKA

Product Code Name

Tubes, vials, systems, serum separators, blood collection

Public Device Record Key

a88f709c-98d5-4289-89ce-897d097846c0

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 09, 2017

Package DI Number

10351688047397

Quantity per Package

10

Contains DI Package

00351688047390

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX