4 laboratories in Germany are accredited by DAKKS under ISO/IEC 17025 to perform ETSI EN 301 489-35 testing. From the accredited scope text: “ETSI EN 301 489-35 V 2.2.1 2019-04 ElectroMagnetic Compatibility ( EMC ) standard for radio equipment and services; Harmonised Standard covering the essential requirements of article 3.1(b) of Directi” “ETSI EN 301 489-35 V2.2.1 ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 35: Specific requirements for Low Power Active Medical Implants (LP-AMI) operating in the”
Nürnberg, DE
ETSI EN 301 489-35 V 2.2.1 2019-04 ElectroMagnetic Compatibility ( EMC ) standard for radio equipment and services; Harmonised Standard covering the essential requirements of article 3.1(b) of Directive 2014/53/EU; Part 35: Specific
Plattling, DE
ETSI EN 301 489-35 V2.2.1 ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 35: Specific requirements for Low Power Active Medical Implants (LP-AMI) operating in the 2 483,5 MHz to 2 500 MHz bands; Ha
Puchheim, DE
ETSI EN 301 489-35 V2.2.1: 2019 Electromagnetic Compatibility (EMC) standard for radio equipment and services; Part 35: Specific requirements for Low Power Active Medical Implants (LP-AMI) operating in the 2 483,5 MHz to 2 500 MHz ba
Straubing, DE
Bereich Norm oder Prüfverfahren / Ausgabestand Titel der Norm oder des Prüfverfahrens Prüfbereich / Einschränkungen TK ETSI EN 301 489 -35 V2.2.1 (2019-04) Electro magnetic Compatibility (EMC) standard for radio equipment and s
This page is a fixed slice of the register: every ETSI EN 301 489-35 scope we hold for Germany. Search narrows it further by city, accreditation body, or a term from the scope text itself.
Search labs in GermanyDeutsche Akkreditierungsstelle (DAKKS) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in Germany.
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.