Pulmeq sp. z o.o.

• Urząd Rejestracji Produktów Leczniczych
  PolandContact the authority →

Devices placed in 32 countries

• Poland18
• Austria8
• Belgium8
• Bulgaria8
• Cyprus8
• Czechia8
• Germany8
• Denmark8
• Estonia8
• Spain8
• Finland8
• France8
• Greece8
• Croatia8
• Hungary8
• Ireland8
• Iceland8
• Italy8
• Liechtenstein8
• Lithuania8
• Luxembourg8
• Latvia8
• Malta8
• Netherlands8
• Norway8
• Portugal8
• Romania8
• Sweden8
• Slovenia8
• Slovakia8
• Türkiye8
• XI8

2 contacts identified

• JM
  JUNOSZA-SZANIAWSKA Marta

  PRRC
  View profile →
• JUNOSZA-SZANIAWSKA Marta
  ensuring that: (a) the conformity of the devices is checked, in accordance with the QMS, before a device is released; (b) the TF and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with in accordance with Article 10(10); (d) the reporting obligations referred to in Articles 87 to 91 are fulfilled; (e) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued
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• — Pulmeq

No certificates registered for this manufacturer.