Catalog Number

-

Brand Name

Portex

Version/Model Number

A1272-17

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

K965017,K965017

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

8f69a236-230f-4811-aad7-b9eefaf90d4b

Public Version Date

November 08, 2019

Public Version Number

5

DI Record Publish Date

January 03, 2017

Package DI Number

10351688001733

Quantity per Package

10

Contains DI Package

00351688001736

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX