Catalog Number

5039

Brand Name

MICRO-MATE®

Version/Model Number

5039

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 30, 2019

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

-

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

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

42973ecb-8e85-48b4-9bd6-2537d3fab03e

Public Version Date

February 27, 2020

Public Version Number

4

DI Record Publish Date

September 20, 2016

Package DI Number

00816329020366

Quantity per Package

12

Contains DI Package

00816329020397

Package Discontinue Date

November 30, 2019

Package Status

Not in Commercial Distribution

Package Type

Box