I-Ritamedtech (Zhongshan) Limited (ebizwa nge-Ritamedtech) yasungulwa ngo-2023. Iyinkampani engaphansi kwe-Hongrita Group egxile ekukhonzeni imboni yezokwelapha, ihlinzeka ngezixazululo eziphelele zokukhiqiza ukubumba zepulasitiki yedivayisi yezokwelapha ye-Class I kuya ku-Class III kanye nezingxenye zokunemba ze-silicone rubber (LSR) kanye namamojula kumakhasimende adumile emhlabeni jikelele.

I-Ritamedtech isebenzisa i-Class 100,000 (ISO 8) GMP Cleanroom eqinisekisiwe kanye ne-Class 10,000 (ISO 7) GMP Laboratory, uhlelo lokupholisa umoya oluhlanzekile oluhlotshiswe nge-HEPA, uhlelo lokuhlanza amanzi, uhlelo lokuqapha imvelo, kanye nezindawo zokuhlanza inzalo ezindaweni zokukhiqiza. Le nkampani igcina amakhono angaphakathi okuhlola inzalo, ukuqinisekiswa kwe-bioburden, kanye nokuhlaziywa kwezinhlayiya, okusekelwa yi-ISO13485 Quality Management System eqinisekisiwe. Lolu hlaka oluhlanganisiwe luqinisekisa ukuhambisana okugcwele ne-Medical Device Good Manufacturing Practice yaseShayina (MDGMP 2014), Imfuneko Yokuphatha Yokukhiqiza Amadivayisi Ezokwelapha Aseptic (YY 0033-2000), Ikhodi Yokuklama Amakamelo Okuhlanza (GB 50073-2013), Ikhodi Yokwakha Nokwamukelwa Kwamagumbi Okuhlanza (GB 50591-2010) kanye ne-US FDA 21 CFR Part 820—Umthethonqubo Wesistimu Yekhwalithi.