QuikRead go® CRP 145215

GUDID 06438115000099

QuikRead go® CRP test is an immunoturbidimetric assay for the in vitro quantitative determination of C-reactive protein (CRP). The test is carried out

Orion Diagnostica Oy

C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry
Primary Device ID06438115000099
NIH Device Record Keyab156e02-ee23-4b00-bf7d-3a86a4268248
Commercial Distribution StatusIn Commercial Distribution
Brand NameQuikRead go® CRP
Version Model Number145215
Catalog Number145215
Company DUNS401656868
Company NameOrion Diagnostica Oy
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+358104261
Emailproduct.support@oriondiagnosti
Phone+358103093000
Emailproduct.support@aidian.eu
Phone+358103093000
Emailproduct.support@aidian.eu
Phone+358103093000
Emailproduct.support@aidian.eu
Phone+358103093000
Emailproduct.support@aidian.eu
Phone+358103093000
Emailproduct.support@aidian.eu
Phone+358103093000
Emailproduct.support@aidian.eu

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS106438115000099 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DCKC-Reactive Protein, Antigen, Antiserum, And Control

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-01

Devices Manufactured by Orion Diagnostica Oy

06438115000006 - Uricult® CLED+Polymyxin / MacConkey2020-02-06 A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.
06438115000013 - Uricult® CLED+Polymyxin /EMB2020-02-06 A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.
06438115000020 - Uricult® CLED/MacConkey2020-02-06 A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.
06438115000037 - Uricult CLED/EMB2020-02-06 A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.
06438115000044 - Uricult® Trio2020-02-06 A dip slide culture method for diagnosing urinary tract infections by demonstrating microbes in urine.
06438115000198 - QuikRead go® Instrument2019-03-11 QuikRead go® instrument has been designed to measure quantitative test results from patient samples using QuikRead go® reagent
06438115000082 - UniQ® PINP RIA2018-07-06 UniQ® PINP RIA is a quantitative radioimmunoassay designed for the measurement of the concentration of intact aminoterminal pro
06438115000099 - QuikRead go® CRP2018-07-06QuikRead go® CRP test is an immunoturbidimetric assay for the in vitro quantitative determination of C-reactive protein (CRP). The test is carried out
06438115000099 - QuikRead go® CRP2018-07-06 QuikRead go® CRP test is an immunoturbidimetric assay for the in vitro quantitative determination of C-reactive protein (CRP).

Trademark Results [QuikRead go]

Mark Image

Registration | Serial
Company
Trademark
Application Date
QUIKREAD GO
QUIKREAD GO
87287059 5255508 Live/Registered
Orion Diagnostica Oy
2017-01-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.