Catalog Number

-

Brand Name

Metromed

Version/Model Number

BC2159

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

9dd24d0e-ad39-4c9c-9c52-6e6c5f3ea0b3

Public Version Date

June 08, 2021

Public Version Number

1

DI Record Publish Date

May 31, 2021

Package DI Number

00813153026748

Quantity per Package

1

Contains DI Package

10813153026745

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-