Catalog Number

-

Brand Name

DUST CAP, 22F

Version/Model Number

1978000

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

62ce0c48-16b3-4c57-bf2b-3f7814cf563a

Public Version Date

February 07, 2022

Public Version Number

2

DI Record Publish Date

October 14, 2021

Package DI Number

05030267006090

Quantity per Package

180

Contains DI Package

05030267057726

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-