Catalog Number

275.00

Brand Name

VYGON

Version/Model Number

275.00

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

BRZ

Product Code Name

Set, blood transfusion

Public Device Record Key

2f2461cd-de56-4f58-b9c8-bd460076647a

Public Version Date

October 22, 2018

Public Version Number

4

DI Record Publish Date

September 13, 2016

Package DI Number

53660812003396

Quantity per Package

8

Contains DI Package

13660812005965

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-