Double Medical Technology Inc.

• DE/CA05 - Behorde fur Justiz und Verbraucherschutz
  GermanyContact the authority →

Devices placed in 32 countries

• Italy651
• Croatia525
• Cyprus516
• Lithuania377
• Spain376
• Czechia359
• Latvia354
• Portugal342
• Romania328
• Poland276
• Slovenia230
• Slovakia223
• Türkiye199
• Bulgaria198
• Greece191
• Hungary186
• Belgium183
• Germany183
• Austria182
• Denmark182
• Estonia182
• Finland182
• France182
• Ireland182
• Iceland182
• Liechtenstein182
• Luxembourg182
• Malta182
• Netherlands182
• Norway182
• Sweden182
• XI182

10 contacts identified

• CY
  CHEN Yubin

  PRRC
  View profile →
• HW
  HUANG Wei

  PRRC
  View profile →
• LJ
  LI Junfeng

  PRRC
  View profile →
• LZ
  LU Zhongwei

  PRRC
  View profile →
• NJ
  NIU Jun

  PRRC
  View profile →
• LU Zhongwei
  In accordance with the European Union Medical Device Regulation (EU) 2017/745 (MDR), ensure the quality management system is in compliance in the most effective manner and in a manner that is proportionate to the risk class and the type of device.
  Hidden
• HUANG Wei
  In accordance with the European Union Medical Device Regulation (EU) 2017/745 (MDR), ensure the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released.
  Hidden
• NIU Jun
  In accordance with the European Union Medical Device Regulation (EU) 2017/745 (MDR), ensure the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released.
  Hidden
• LEE Jeffrey
  1.Ensure technical documentation and the EU Declaration of Conformity are prepared and maintained per EU MDR 2017/745. 2.Ensure post-market surveillance (PMS) obligations are fulfilled and the PMS system is implemented and maintained per EU MDR 2017/745 and the PMS Control Procedure. 3.Ensure a signed statement confirms the investigational device conforms to general safety and performance requirements and all precautions for subject health and safety are taken, per EU MDR 2017/745.
  Hidden
• CHEN Yubin
  In accordance with the European Union Medical Device Regulation (EU) 2017/745 (MDR), ensure that the vigilance reporting obligations are fulfilled in compliance with Articles 87 to 91 of the European Union Medical Device Regulation (EU) 2017/745 (MDR), and Control Procedure of the European Vigilance System.
  Hidden

• TÜV SÜD Product Service GmbH — 1 certificate — Double Medical Technology Inc.
• UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş. — 1 certificate — Double Medical Technology Inc.
• Shanghai International Holding Corp. GmbH(Europe) — represents — Double Medical Technology Inc.
• — represents — Double Medical Technology Inc.
• — Double Medical Technology Inc.
• — Double Medical Technology Inc.
• — Double Medical Technology Inc.
• — Double Medical Technology Inc.
• — Double Medical Technology Inc.