Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification
Since 2001
45000㎡
251
ANVISA, Росздравнадзор, Japan Certificate of Foreign Medical Device Manufacturer, MHRA, CE, NBC Universal, BSCI (Overall Rating B), GB/T29490, ISO45001, ISO14001, ISO13485, CE MDR Quality Management System Certificate (EU)2017/745, US FDA 510(k) Premarket Notification, US FDA 510 (k) Premarket Notification