Catalog Number

-

Brand Name

BiTrac Select

Version/Model Number

313-9524

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"

-

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

K023683,K023683

Product Code

BZD

Product Code Name

Ventilator, Non-Continuous (Respirator)

Public Device Record Key

5fb39b54-abca-4285-a261-69294813f1b2

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 31, 2017

Package DI Number

10841470111097

Quantity per Package

10

Contains DI Package

00841470111090

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-