Haiyan Kangyuan Instrumentum Medical Co., Ltd. feliciter consecutus est Regulationem Unionis Europaeae Medical Fabrica 2017/745 (relatum ad "MDR") certificationem CE die 19 mensis Iulii anno 2023, numerus certificationis 6122159CE01, certificationis ambitus est Catheters urinariorum pro uno usu ( Foley) Speciatim includit 2 modo catheter silicone foley, 3 modo silicone foley catheter, 2 modo silicone foley catheter cum apice tiemann et 3 modo catheter silicone foley cum apice coude.Nunc, Kangyuan Medical producta MDR transiit;

Endotracheal Tubuli pro uno usu

Catheters sterilis suctionis pro uno usu

Oxygen Masks for Single Use;

Cannulas nasi Oxygen pro Unius Usus;

Guedel Airlines for Single Use;

Laryngeal Mask Airways;

Anesthesia Masks for Single Use;

Respiratio Filtra pro Singulo Usu;

Spirans Circuitus pro Singulo Usu;

Catheters urinarii pro uno usu (Foley).

EU MDR certificatio ostendit Kangyuan Medical producta requisitis occurrere novissimae EU medici machinae dispositionis 2017/745, condiciones recentissimas accessus mercatus EU habere et pergere posse licite venditis in mercatis transmarinis pertinentibus, solido fundamento pro ulterius forum Europae intrantes et processum internationalizationis promovent.