Sdělení k ověřování vah
pro uživatele a žadatele o jejich ověření v době a po skončení nouzového stavu vyhlášeného v ČR v důsledku šíření nemoci COVID-19
You are here
News
CMI as a Notified Body for EU MDR
CMI has entered the final phase of its preparations for conformity assessment of medical devices under the new EU Regulation MDR. The CMI application to become a Notified Body for the EU Regulation MDR will be submitted still by the end of 2020 with the scope of MD codes given here.
Participation in the certification system OIML-CS
Recently, the CMI scope has been extended by adding fuel dispensers, AWIs and gasmeters to Scheme A - see https://www.oiml.org/en/oiml-cs/oiml-issuing-authorities/cmi-czech-republic. By the end of the year steps will be taken to add level gauges (OIML R 85) and compressed gaseous fuel systems (OIML R 139 - CNG, hydrogen).
- ‹ předchozí
- 26 of 42
- následující ›