Catalog Number

-

Brand Name

Portex

Version/Model Number

8506F

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

K014115,K014115

Product Code

BTM

Product Code Name

Ventilator, emergency, manual (resuscitator)

Public Device Record Key

8051dec0-5088-4599-8502-a4fd654a54be

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 01, 2015

Package DI Number

35019315060940

Quantity per Package

12

Contains DI Package

15019315060946

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX