Catalog Number

-

Brand Name

MP Vial Adapter 13 mm

Version/Model Number

8070150

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 30, 2018

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

82cc2ed0-0982-4a1e-8b40-65907b9de6c5

Public Version Date

February 03, 2022

Public Version Number

8

DI Record Publish Date

May 01, 2016

Package DI Number

27290108240683

Quantity per Package

4

Contains DI Package

17290108240686

Package Discontinue Date

September 30, 2018

Package Status

Not in Commercial Distribution

Package Type

-