Catalog Number

-

Brand Name

iPro™ 2

Version/Model Number

MMT-7741

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

P150029,P150029,P980022

Product Code

MDS

Product Code Name

Sensor, glucose, invasive

Public Device Record Key

13065db5-7444-4960-bbcf-27b76f4ba3a7

Public Version Date

August 30, 2022

Public Version Number

6

DI Record Publish Date

October 30, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-