Aidian Oy

Address:KOIVU-MANKKAAN TIE 6B,ESPOO Uusimaa,FI

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- Catalog Number : 1003

Device Description : A dip slide culture method for the detection of bacteriuria and the presumptive A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.

Device Class :

Duns Number: 401656868

Premarket Exempt : Yes

Product Code : JSI

Prescription Use : Yes

Device Count : 10

- Catalog Number : 1002

Device Description : A dip slide culture method for the detection of bacteriuria and the presumptive A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.

Device Class :

Duns Number: 401656868

Premarket Exempt : Yes

Product Code : JSI

Prescription Use : Yes

Device Count : 10

- Catalog Number : 1001

Device Description : A dip slide culture method for the detection of bacteriuria and the presumptive A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.

Device Class :

Duns Number: 401656868

Premarket Exempt : Yes

Product Code : JSH

Prescription Use : Yes

Device Count : 10

- Catalog Number : 1000

Device Description : A dip slide culture method for the detection of bacteriuria and the presumptive A dip slide culture method for the detection of bacteriuria and the presumptive identification of uropathogens.

Device Class :

Duns Number: 401656868

Premarket Exempt : Yes

Product Code : JSH

Prescription Use : Yes

Device Count : 10

- Catalog Number : 68197

Device Description : A dip slide culture method for diagnosing urinary tract infections by demonstrat A dip slide culture method for diagnosing urinary tract infections by demonstratingmicrobes in urine.

Device Class :

Duns Number: 401656868

Premarket Exempt : Yes

Product Code : JSI

Prescription Use : Yes

Device Count : 10

- Catalog Number : 67034

Device Description : UniQ® PINP RIA is a quantitative radioimmunoassay designed for the measurement o UniQ® PINP RIA is a quantitative radioimmunoassay designed for the measurement of the concentrationof intact aminoterminal propeptide of type I procollagen, an indicator of osteoblastic activity, in human serum.

Device Class : 2

Duns Number: 401656868

Premarket Exempt : No

Product Code : CIN

Prescription Use : Yes

Device Count : 1

- Catalog Number : 145215

Device Description : QuikRead go® CRP test is an immunoturbidimetric assay for the in vitro quantitat QuikRead go® CRP test is an immunoturbidimetric assay for the in vitro quantitative determination of C-reactive protein (CRP). The test is carried out by means of the QuikRead go® instrument.

Device Class : 2

Duns Number: 401656868

Premarket Exempt : No

Product Code : DCK

Prescription Use : Yes

Device Count : 1

- Catalog Number : 145216

Device Description : QuikRead go® CRP Verification Set is designed to be used for calibration verific QuikRead go® CRP Verification Set is designed to be used for calibration verification and for method validation of the QuikRead go® CRP system. It is intended for use with the QuikRead go® CRP test and the QuikRead go® instrument.

Device Class : 1

Duns Number: 401656868

Premarket Exempt : No

Product Code : JJX

Prescription Use : Yes

Device Count : 1

- Catalog Number : 145217

Device Description : QuikRead go® CRP Control Set is intended for use as assayed quality-control mate QuikRead go® CRP Control Set is intended for use as assayed quality-control material for monitoring the performance of the quantitative QuikRead go CRP assay with the QuikRead go Instrument.

Device Class : 1

Duns Number: 401656868

Premarket Exempt : No

Product Code : JJX

Prescription Use : Yes

Device Count : 1

- Catalog Number : 145218

Device Description : QuikRead go® instrument has been designed to measure quantitative test results f QuikRead go® instrument has been designed to measure quantitative test results from patient samples using QuikRead go® reagent kits.

Device Class : 1

Duns Number: 401656868

Premarket Exempt : No

Product Code : JJQ

Prescription Use : Yes

Device Count : 1