PHOENIX S.R.L.

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

Devices placed in 32 countries

• Italy451
• France450
• Germany443
• Spain443
• Greece419
• Austria278
• Belgium278
• Bulgaria278
• Cyprus278
• Czechia278
• Denmark278
• Estonia278
• Finland278
• Croatia278
• Hungary278
• Ireland278
• Iceland278
• Liechtenstein278
• Lithuania278
• Luxembourg278
• Latvia278
• Malta278
• Netherlands278
• Norway278
• Poland278
• Portugal278
• Romania278
• Sweden278
• Slovenia278
• Slovakia278
• Türkiye278
• XI278

4 contacts identified

• PA
  PIVA Annarosa

  PRRC
  View profile →
• PF
  PRANDINI Federico

  PRRC
  View profile →
• PRANDINI Federico
  ensuring that: - the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; - the post-market surveillance obligations are complied with in accordance with Article 10(10) of MDR; - the reporting obligations referred to in Articles 87 to 91 of MDR are fulfilled; - in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of MDR is issued.
  Hidden
• PIVA Annarosa
  ensuring that: - 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

• PHOENIX S.R.L. — IT-MF-000023426
• PHOENIX S.R.L. — IT-PR-000046613
• ICIM S.P.A. — 1 certificate — PHOENIX S.R.L.
• PIVA Annarosa — PHOENIX S.R.L.
• PRANDINI Federico — PHOENIX S.R.L.