Catalog Number

-

Brand Name

MP Vial Adapter 13mm

Version/Model Number

8070149

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,K130179

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

130012eb-b736-4ed9-9d89-0fc70fdfe9c0

Public Version Date

July 23, 2020

Public Version Number

9

DI Record Publish Date

June 06, 2017

Package DI Number

27290108240799

Quantity per Package

3

Contains DI Package

17290108240792

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-