Catalog Number

-

Brand Name

Vented Vial Adapter Transfer Device

Version/Model Number

8073030

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

K062482,K062482,K062482

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

0c9b529d-45b2-4278-a921-71f20bf2547b

Public Version Date

August 09, 2019

Public Version Number

6

DI Record Publish Date

May 01, 2016

Package DI Number

27290108240751

Quantity per Package

4

Contains DI Package

17290108240754

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-