Catalog Number

-

Brand Name

n.a.

Version/Model Number

60-12-200

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

BZA

Product Code Name

Connector, Airway (Extension)

Public Device Record Key

9e21fa76-113e-4a02-8bce-ae859f7a1d06

Public Version Date

September 06, 2022

Public Version Number

3

DI Record Publish Date

August 26, 2020

Package DI Number

14250105604457

Quantity per Package

10

Contains DI Package

04250105604450

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-