Ceracarta S.p.A.

• Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
  ItalyContact the authority →

No certificates registered for this manufacturer.

Devices placed in 32 countries

• Belgium41
• Bulgaria41
• Cyprus41
• Czechia41
• Germany41
• Denmark41
• Estonia41
• Spain41
• Finland41
• France41
• Greece41
• Croatia41
• Hungary41
• Ireland41
• Iceland41
• Italy41
• Liechtenstein41
• Lithuania41
• Luxembourg41
• Latvia41
• Malta41
• Netherlands41
• Norway41
• Poland41
• Portugal41
• Romania41
• Sweden41
• Slovenia41
• Slovakia41
• Türkiye41
• XI41
• Austria40

4 contacts identified

• TF
  TANFI FRANCESCA

  PRRC
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• VD
  VALENTINI DANIELE

  PRRC
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• TANFI FRANCESCA
  1)The technical documentation and the EU declaration of conformity are drawn up and up-to-date; 2)The post-market surveillance obligations referred to in the Article are met 10, paragraph 10 (MDR 2017/745). 3)The reporting obligations referred to in articles 87 to 91 (MDR 2017/745). 4)In the case of devices under investigation, the declaration referred to in the annex is issued XV, chapter II, point 4.1. (MDR 2017/745).
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• VALENTINI DANIELE
  The conformity of the devices is adequately controlled in accordance with the system quality management whereby devices are manufactured before a device is released.
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• Ceracarta S.p.A. — IT-IM-000032501
• Ceracarta S.p.A. — IT-MF-000033859
• TANFI FRANCESCA — Ceracarta S.p.A.
• VALENTINI DANIELE — Ceracarta S.p.A.