Catalog Number

BN-208

Brand Name

VYGON

Version/Model Number

BN-208

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

K021395,K021395

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

6b1f6941-4b9c-4b20-958f-b6bf63a1b8dd

Public Version Date

February 05, 2020

Public Version Number

1

DI Record Publish Date

January 28, 2020

Package DI Number

30849884003674

Quantity per Package

50

Contains DI Package

00849884003673

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-