Ritamedtech (Zhongshan) Limited (lea ua taʻua mulimuli ane o Ritamedtech) na faavaeina i le 2023. O se lala o le Hongrita Group faʻapitoa i le tautuaina o le falemaʻi, tuʻuina atu fofo faʻapipiʻi atoatoa mo Vasega I i le Vasega III masini faʻafomaʻi palasitika ma paʻu silicone vai (LSR) saʻo vaega ma modules mo tagata lauiloa i le lalolagi atoa.

Ritamedtech faagaoioia se Vasega faamaonia 100,000 (ISO 8) GMP Cleanroom ma se Vasega 10,000 (ISO 7) GMP Laboratory, faʻapipiʻiina HEPA-filtered mama ea-conditioning system, vai faʻamamaina faiga, faiga mataʻituina le siosiomaga, ma sterilization nofoaga mo nofoaga gaosiga. O lo'o fa'atumauina e le kamupani le agava'a i totonu o le fale mo su'esu'ega fa'ama'i, fa'amaoniaina o le bioburden, ma le su'esu'eina o vaega, lagolagoina e le ISO13485 Quality Management System fa'amaonia. O lenei auivi tu'ufa'atasia e fa'amautinoaina le tausisia atoatoa o le Fa'ata'ita'iga Lelei o Mea Fa'afoma'i a Saina (MDGMP 2014), Mana'oga Fa'atonu mo le Fa'aaogāina o Mea Fa'afoma'i Aseptic (YY 0033-2000), Fa'ailoga mo le Fuafuaga o Fale Mama (GB 50073-2013), Fa'ailoga mo le Fausiaina ma le Taliaina o Fale Fa'amama (GB-201 FDA) ma le US Parts 501. 820—Tulafono Fa'atonu Fa'atonu.