Class 10K ISO-13485-2016 Certified Clean Room Facility

Calss 10K clean room facility, certified with ISO-13485-2016 and sFDA GMP system, capable for interventional device manfacturing and testing  including tubing extrusion, part injection molding, balloon blowing, laser welding, final product assembly, packaging; biostability test, microbiology study  and other balloon catheter related chemical andrphysical testing et al.