Catalog Number

-

Brand Name

MP Vial Adapter 13 mm

Version/Model Number

8070142

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

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

43ce3043-0e6a-4b2c-8f97-54fbff14ab65

Public Version Date

July 23, 2020

Public Version Number

7

DI Record Publish Date

May 01, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-