GE Vingmed Ultrasound AS

• The Norwegian Medical Products Agency
  NorwayContact the authority →

Devices placed in 32 countries

• Austria47
• Germany42
• Spain42
• France42
• Norway42
• Belgium41
• Bulgaria41
• Cyprus41
• Czechia41
• Denmark41
• Estonia41
• Finland41
• Greece41
• Croatia41
• Hungary41
• Ireland41
• Iceland41
• Italy41
• Liechtenstein41
• Lithuania41
• Luxembourg41
• Latvia41
• Malta41
• Netherlands41
• Poland41
• Portugal41
• Romania41
• Sweden41
• Slovenia41
• Slovakia41
• XI41
• Türkiye38

No certificates registered for this manufacturer.

3 contacts identified

• RJ
  RONANDER Jon

  PRRC
  View profile →
• THOLLEFSEN Jan Tore
  15.3 (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 15.3 (e) investigational devices conform to the general safety and performance requirements apart from the aspects covered by the clinical investigation and that, with regard to those aspects, every precaution has been taken to protect the health and safety of the subject.
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• RONANDER Jon
  15.3 (a) 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; 15.3 (c) the post-market surveillance obligations are complied with in accordance with EU MDR Article 10(10); 15.3 (d) the reporting obligations referred to in EU MDR Articles 87 to 91 are fulfilled;
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• GE Vingmed Ultrasound AS — NO-IM-000000554
• GE Vingmed Ultrasound AS — NO-MF-000000553
• RONANDER Jon — GE Vingmed Ultrasound AS