EPTIS
BAM Logo

Urine chemistry, qualitative

[Vizelet rutin, kvalitatív]

EPTIS Ringversuch Nr. 1255810 | Letze Änderung 2026-03-20 | URL: https://www.eptis.bam.de/pts1255810 https://www.eptis.bam.de/pts1255810

Name des Anbieters
Name des Anbieters QualiCont In Vitro Diagnostic Quality Control Nonprofit Ltd. QualiCont In Vitro Diagnostic Quality Control Nonprofit Ltd.
Ansässig in Hungary
Sprache(n) English, Hungarian
Anmerkungen The test samples are basically intended for semi-quantitative urine chemistry with diagnostic test strips. The results displayed on the test strip should be reported. In proficiency testing, different results may be obtained from a given sample based on the sensitivity and specificity of the different test strips, and this is taken into account in the target values and the acceptable range. Therefore, the test strip results should be reported regardless of the sediment test results! In daily routine work, a correct result is reported for human samples, i.e. after the sediment test, the false positive or false negative result of the test strip for cellular elements should be adjusted if necessary. If two sets of samples are required for the determination, please order double amount! QualiCont has had accredited status as the QualiCont as a Proficiency Test Provider complies with the criteria of MSZ EN ISO/IEC 17043:2010 standard since 26 March 2014. The QualiCont has been accredited according to the MSZ EN ISO/IEC 17043:2023 standard since 18 December 2025. Our Company is a Proficiency Testing Provider Organisation accredited by NAH (National Accreditation Authority) under the NAH-8-0002/2023 registration number. As the result of the accreditation process performed by NAH, our Company has accredited status until 9 March 2028. QualiCont Nonprofit Kft. has been operating its quality management system since 2001. Our Company successfully passed the renewal audit on 6th May, 2025. The certificate is valid until 28 May 2028. Our Company has been assessed and certified as meeting the requirements of ISO 9001:2015 standard for the following activities: Planning, organization and management of proficiency testing (external quality assessment) and the related supporting services for in vitro medical diagnostic laboratories and investigators on other human and veterinary medicine.
Klassifizierung
Produktgruppen Health care / medical devices
Human test material
Prüfgebiete Medical analysis
Technische Einzelheiten
Prüfobjekt Prüfeigenschaft Prüfmethode
2 samples of 10 mL liquid human urine each Ascorbic acid Test strip
Bilirubin Test strip
Erythrocyte (RBC) Test strip
Microscopic examination/urinary sediment
Glucose Test strip
HCG Test strip
Agglutination test
Ketone bodies Test strip
Leucocyte (WBC) Test strip
Microscopic examination/urinary sediment
Microalbumin Test strip
Nitrite Test strip
PH Test strip
Potentiometry (glass electrode)
Specific gravity Test strip
Areometer/urometer
Protein Test strip
Qualitative determination with sulfosalicilic acid
Qualitative determination with acetic acid-boiling method
Urobilinogen Test strip
Ehrlich reagent
Erythrocyte (RBC) in the sediment Microscopic analysis
Instrumental analysis
Flow cytometric method
Leucocyte (WBC) in the sediment Microscopic analysis
Instrumental analysis
Flow cytometric method
Crytals in the sediment Microscopic analysis
Instrumental analysis
Flow cytometric method
Bacterium in the sediment Microscopic analysis
Instrumental analysis
Flow cytometric method
Epithelial cells in the sediment Microscopic analysis
Instrumental analysis
Flow cytometric method
Cylinders in the sediment Microscopic analysis
Instrumental analysis
Flow cytometric method
Ringversuchsziele
Zielgruppe des Ringversuchs In vitro medical laboratories & general practitioners (adults & children)
Relevante Rechtsvorschriften oder Normen CLSI GP16-A3 – Urinalysis ILAC_G8:09/2019 – Guidelines on Decision Rules and Statements of Conformity ISO 15189 – Medical laboratories – Requirements for quality and competence ISO/TS20658:2017 – Medical laboratories – Requirements for collection, transport, receipt and handling of samples VIM3 – Vocabulaire International de Métrologie WHO – Guidance on regulations for the Transport of Infectious Substances The EFLM European Urinalysis Guideline 2023
Weitere Ziele validation of testing methods
Teilnehmerzahl
Anbieter unabhängig überprüft (akkreditiert, benannt, anerkannt)

Akkreditiert durch NAH (National Accreditation Authority) auf der Grundlage von ISO/IEC 17043:2010

Die Durchführung des Ringversuchs ist in Auftrag gegeben durch
Kosten
Teilnahmegebühr on demand
Regelmässig durchgeführt Ja (four times a year)
Der Ringversuch wird durchgeführt seit 1997
Kontaktdaten des Anbieters
Anbieter Kontaktperson
QualiCont In Vitro Diagnostic Quality Control Nonprofit Ltd.
Feketesas u. 19-21. I/7
6720 Szeged
Hungary

Telefon: +36 30 462 5864
Fax:
Web: http://www.qualicont.com/qc/index_en.html http://www.qualicont.com/qc/index_en.html
Ms. Eszter Mezey
Telefon: +36 30 462 5864
Fax:
E-Mail: mail@qualicont.com mail@qualicont.com
Haben Sie einen Fehler entdeckt? Bitte wenden Sie sich an den zuständigen EPTIS Koordinator für Hungary, Ms Eszter Mezey. Ms Eszter Mezey.
Haben Sie Fragen? Senden Sie uns eine E-Mail: eptis@bam.de.
Anwendungsversion: 1.23-SNAPSHOT.20230502124635-7925ae379a631fc1ececff45d2921c8db38877d5