Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)
Since 2004
5000 m²
150
Certificate for Exportation of Medical Products, FDA, EN ISO 13485:2016 Medical Device Quality Management System, Notified Body Confirmation Letter (MDR Transition Document)