Catalog Number

-

Brand Name

NA

Version/Model Number

L1(D19)

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

BZO

Product Code Name

Set, Tubing And Support, Ventilator (W Harness)

Public Device Record Key

2f129831-3314-4197-882b-4ea5ad0584ff

Public Version Date

May 20, 2020

Public Version Number

2

DI Record Publish Date

April 06, 2020

Package DI Number

16948538362263

Quantity per Package

30

Contains DI Package

06948538362266

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-