Catalog Number

-

Brand Name

n.a.

Version/Model Number

60-12-400

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

-

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

78f69ffa-2285-4356-bf60-708897ea9db7

Public Version Date

September 06, 2022

Public Version Number

3

DI Record Publish Date

September 02, 2020

Package DI Number

14250105600640

Quantity per Package

10

Contains DI Package

04250105600643

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-