Catalog Number

-

Brand Name

Portex

Version/Model Number

A4220-17

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 13, 2019

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

K965017,K965017

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

e3af88b4-81d4-4e3b-aaf1-1561d1776bfe

Public Version Date

October 08, 2019

Public Version Number

5

DI Record Publish Date

December 13, 2016

Package DI Number

30351688082767

Quantity per Package

10

Contains DI Package

20351688082760

Package Discontinue Date

August 13, 2019

Package Status

Not in Commercial Distribution

Package Type

Case