Catalog Number

-

Brand Name

MP Vial Adapter

Version/Model Number

8070150

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

K130179,K130179

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

a2d2569f-6dcc-4643-ae7d-25d79c6b8713

Public Version Date

July 23, 2020

Public Version Number

6

DI Record Publish Date

April 23, 2018

Package DI Number

27290108241192

Quantity per Package

156

Contains DI Package

37290108241199

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-