Catalog Number

VM-1021

Brand Name

VACSURE SAFETY MULTI-SAMPLE NEEDLE

Version/Model Number

VM-1021

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

-

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

4c145367-78d4-48ec-8c07-a1cf1229e93f

Public Version Date

April 05, 2021

Public Version Number

3

DI Record Publish Date

January 23, 2021

Package DI Number

10850014448001

Quantity per Package

50

Contains DI Package

00850014448004

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Box