Catalog Number

-

Brand Name

Bioseal

Version/Model Number

19711/10

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GAZ

Product Code Name

TUBING, NONINVASIVE

Public Device Record Key

eba4eed3-cb28-45a9-9bd9-9a4e6cec68e8

Public Version Date

February 03, 2020

Public Version Number

1

DI Record Publish Date

January 24, 2020

Package DI Number

10630094197118

Quantity per Package

10

Contains DI Package

00630094197111

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case