4 laboratories in Finland are accredited by FINAS under ISO/IEC 17025 to perform IEC 61326-1 testing. From the accredited scope text: “IEC 61326-1:2021 Tampere Sähköiset ja elektroniset laitteet Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement EN IEC 55011:” “IEC 61326-1 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment IEC 61326-2-6 On the f”
Tampere, FI
IEC 61326-1:2021 Tampere Sähköiset ja elektroniset laitteet Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement EN IEC 55011:2025 EN 55011:2016 + A1:2017 + A11:2
Jyväskylä, FI
T298/M23/2025 Liite 1 / Appendix 1 Sivu / Page 6(23) Vaatimus/Requirement SFS-EN ISO/IEC 17025:2017 17.12.2025 Päätöksen päiväys / Date of decision 22.07.2028 Päätöksen viimeinen voimassaolopäivä / Date of expiry www.finas.fi Voimass
Oulu, FI
T290/A21/2025 Liite 1 / Appendix 1 Sivu / Page 7(24) Vaatimus/Requirement SFS-EN ISO/IEC 17025:2017 30.10.2025 Päätöksen päiväys / Date of decision 31.12.2029 Päätöksen viimeinen voimassaolopäivä / Date of expiry www.finas.fi Voimassaoleva
Helsinki, FI
IEC 61326-1 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment IEC 61326-2-6 On the following types of products/equi
This page is a fixed slice of the register: every IEC 61326-1 scope we hold for Finland. Search narrows it further by city, accreditation body, or a term from the scope text itself.
Search labs in FinlandFinnish Accreditation Service (FINAS) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in Finland.
ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Accreditation to this standard provides independent confirmation that a laboratory operates a quality management system and is technically competent to produce valid results within its declared scope.