Catalog Number

AMS-200

Brand Name

VYGON

Version/Model Number

AMS-200

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

K012157,K012157

Product Code

FMG

Product Code Name

Stopcock, i.V. Set

Public Device Record Key

1cfbb86e-0c16-4d59-8539-afb9c22eb0fe

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 01, 2016

Package DI Number

38498840000770

Quantity per Package

100

Contains DI Package

08498840000779

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-