Nhungamiro yeKumaka lenzi dzemaziso

Nekuenderera mberi kwekuvandudzwa kwezvinodiwa zvemhando yevatengi, zvinodiwa zvevanhu zvema lens optical zvinovandudzwawo zvishoma nezvishoma, panguva imwecheteyo, zvinodiwa nenyika zvema lens optical zviri kuwedzerawo kuomarara.Nzira yekuziva sei kunaka kwayo chiratidzo nekukurumidza?Nhasi tichatarisa iyo optical lens zviyero uye zvinoenderana nekumaka zvinodikanwa munyika dzinoverengeka.

Sangano reEuropean Union
European Union inoda kuti malenzi emaziso anofanirwa kutevedzera Medical Devices Regulation (EU) 2017/745 uye anopihwa certification seanokwanisa.Kuti upinde mumusika weEU zvakanaka, chiratidzo che "CE" chinogona kuwedzerwa
Britain
Mushure meBrexit, Great Britain inoda kuti lenzi dzemaziso dzinofanira kuenderana neMitemo yeMedical Devices Regulations 2002 uye inopihwa certification kuti inokwanisa isati yawedzera chiratidzo che "UKCA" kuti ipinde mumusika wemuno zvakanaka.
United States
MuUnited States, lenzi dzemaziso dzinodzorwawo zvakanyanya semidziyo yekurapa, uye mhando yavo inofanirwa kuzadzisa zvinodiwa neFederal Food and Drug Administration (FDA) (21 CFR 801.410) isati yatengeswa kunze kwenyika.
China
Musika wepamba unofanirwa kusangana nezvinodiwa zveGB/T 38005-2019 standard.
EUROLAB Chigadzirwa Performance Appraisal - chitupa chekuita kuti vatengi vanzwisise nekungotarisa.Vagadziri veOptical lens vanogona kuverengera maitiro ekuita kwezvigadzirwa zvavo pachitupa ichi kuratidza kusarudzika kwezvigadzirwa, kuitira kuwedzera nzvimbo yekutengesa yezvigadzirwa.