Catalog Number

-

Brand Name

TUBE MANAGEMENT CLIP SYSTEM

Version/Model Number

2316000

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

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

db1aac18-0d78-441e-9435-0a97b9929d50

Public Version Date

February 07, 2022

Public Version Number

2

DI Record Publish Date

October 14, 2021

Package DI Number

05030267092307

Quantity per Package

12

Contains DI Package

05030267092291

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-