Catalog Number

RPRC

Brand Name

Exact Diagnostics

Version/Model Number

RPRC

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 05, 2021

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

OHQ

Product Code Name

Multi-Analyte Controls Unassayed

Public Device Record Key

29f78981-92c9-4b97-b43a-f9674a1ed669

Public Version Date

October 11, 2021

Public Version Number

2

DI Record Publish Date

September 19, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-