I-Ritamedtech (Zhongshan) Limited (emva koku ibizwa ngokuba yi-Ritamedtech) yasekwa ngo-2023. Yi-subsidiary ye-Hongrita Group ekhethekileyo ekukhonzeni ishishini lezonyango, ibonelela ngezisombululo ezibanzi zemveliso yeKlasi yoku-I ukuya kuHlelo lwe-III iiplastiki zesixhobo sonyango kunye nerabha elulwelo yerabha (LSR) kunye neemodyuli ezichanekileyo kubathengi abaziwayo kwihlabathi.

I-Ritamedtech isebenzisa i-Classified Class 100,000 (ISO 8) GMP Cleanroom kunye neClass 10,000 (ISO 7) GMP Laboratory, enezixhobo ze-HEPA-filtered clean air-conditioning system, inkqubo yokucoca amanzi, inkqubo yokubeka iliso kwendalo, kunye nezixhobo zokuvala inzalo kwiindawo zokuvelisa. Inkampani igcina amandla angaphakathi okuvavanya ubunyumba, ukuqinisekiswa komthwalo webhayoloji, kunye nohlalutyo lwenxalenye, exhaswa yiNkqubo yoLawulo loMgangatho we-ISO13485 eqinisekisiweyo. Esi sikhokelo esihlangeneyo siqinisekisa ukuthotyelwa ngokupheleleyo kunye neChina yeMedical Medical Practice yaseChina (MDGMP 2014), iMfuneko yoLawulo lwe-Aseptic Medical Device Manufacturing (YY 0033-2000), iKhowudi yoYilo lwamagumbi okucoca (i-GB 50073-2013), iKhowudi ye-5000 yoKwakha kunye ne-1GB ye-2013 ye-US ecocekileyo kunye ne-Acceptance. I-FDA 21 CFR Icandelo le-820-Ulawulo lweNkqubo yoBulunga.