TRUEtrack - LEADER TRUEtrack PRE-PACK - TRIVIDIA HEALTH, INC.

Duns Number:151810868

Device Description: LEADER TRUEtrack PRE-PACK

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More Product Details

Catalog Number

A4002-75

Brand Name

TRUEtrack

Version/Model Number

TRUEtrack PRE-PACK

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 06, 2017

Issuing Agency

In GS1

Product Characteristics

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K032657

Product Code Details

Product Code

CGA

Product Code Name

Glucose Oxidase, Glucose

Device Record Status

Public Device Record Key

932c0478-9e76-42ef-9b4d-c71bbc32cb66

Public Version Date

November 01, 2021

Public Version Number

4

DI Record Publish Date

September 20, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"TRIVIDIA HEALTH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 25
2 A medical device with a moderate to high risk that requires special controls. 22