I-Ritamedtech (Zhongshan) Limited (ebizwa ngokuba yiRitamedtech) yasungulwa ngo-2023. Yinkampani engaphantsi kweHongrita Group egxile ekukhonzeni ishishini lezonyango, ibonelela ngezisombululo ezipheleleyo zemveliso yokubumba kwiiplastiki zezixhobo zonyango zeClass I ukuya kwiClass III kunye nezixhobo zokuchaneka kwerabha yesilicone (LSR) kunye neemodyuli zabathengi abadumileyo kwihlabathi liphela.

I-Ritamedtech isebenzisa iKlasi 100,000 (ISO 8) GMP Cleanroom eqinisekisiweyo kunye neKlasi 10,000 (ISO 7) GMP Laboratory, inkqubo yomoya ococekileyo ecocekileyo efakwe i-HEPA-filtered, inkqubo yokucoca amanzi, inkqubo yokujonga okusingqongileyo, kunye neendawo zokubulala iintsholongwane kwiindawo zemveliso. Le nkampani igcina amandla angaphakathi okuvavanya ukungasebenzi kakuhle, ukuqinisekiswa komthwalo wezinto eziphilayo, kunye nohlalutyo lwamasuntswana, exhaswa yiNkqubo yoLawulo loMgangatho ye-ISO13485 eqinisekisiweyo. Olu lwakhiwo ludibeneyo luqinisekisa ukuthotyelwa ngokupheleleyo yi-China's Medical Device Good Manufacturing Practice (MDGMP 2014), iMfuneko yoLawulo lwe-Aseptic Medical Device Manufacturing (YY 0033-2000), iKhowudi yoYilo lweeCleanrooms (GB 50073-2013), iKhowudi yoKwakhiwa kunye noKwamkelwa kweeCleanrooms (GB 50591-2010) kunye ne-US FDA 21 CFR Part 820—Quality System Regulation.