Catalog Number

VYCIS006

Brand Name

VYGON

Version/Model Number

VYCIS006

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

K011336,K011336

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

ee5a4365-9713-48b4-addd-5302875e13f8

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

July 28, 2017

Package DI Number

38498840010892

Quantity per Package

50

Contains DI Package

08498840010891

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-