Catalog Number

PA401

Brand Name

N/A

Version/Model Number

PA401

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

1c8888c4-94b7-495e-8b27-d780db23722a

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 01, 2017

Package DI Number

10607411944106

Quantity per Package

30

Contains DI Package

00607411944109

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-