Catalog Number

PB402

Brand Name

N/A

Version/Model Number

PB402

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

-

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

BZD

Product Code Name

VENTILATOR, NON-CONTINUOUS (RESPIRATOR)

Public Device Record Key

9da199d5-8f9c-4b84-b85a-c6aa03ec7496

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 01, 2017

Package DI Number

10607411944113

Quantity per Package

30

Contains DI Package

00607411944116

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-