Catalog Number

-

Brand Name

MicroPro™

Version/Model Number

TPF100L

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

LYY

Product Code Name

Latex Patient Examination Glove

Public Device Record Key

4eb98b89-ad55-4ee0-b2fb-33aeab6e35be

Public Version Date

March 17, 2022

Public Version Number

2

DI Record Publish Date

May 31, 2021

Package DI Number

00649531132066

Quantity per Package

10

Contains DI Package

00649531010364

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case