Catalog Number

-

Brand Name

CONNECTOR 22M - 22M, WITH MDI INSERT

Version/Model Number

1966001

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

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

ca1a8da1-0ea1-4796-a7f7-24632b5bf6bf

Public Version Date

February 07, 2022

Public Version Number

2

DI Record Publish Date

October 14, 2021

Package DI Number

05030267005680

Quantity per Package

100

Contains DI Package

05030267057474

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-