Pharmaplast

• Health Products Regulatory Authority, Medical Devices Department
  IrlandeContacter l’autorité →

Dispositifs placés dans 32 pays

• Allemagne3823
• Pologne1347
• Grèce1238
• Hongrie1140
• Italie1100
• Roumanie1088
• Suède1088
• Chypre1066
• Espagne1065
• Portugal1053
• Bulgarie1032
• Pays-Bas1030
• Irlande1029
• XI1020
• France1018
• Belgique1017
• Tchéquie1017
• Autriche1016
• Danemark1016
• Estonie1016
• Finlande1016
• Croatie1016
• Islande1016
• Liechtenstein1016
• Lituanie1016
• Luxembourg1016
• Lettonie1016
• Malte1016
• Norvège1016
• Slovénie1016
• Slovaquie1016
• Turquie1016

7 contacts identifiés

• AR
  ADEL Rojeh

  PCVRR
  Voir le profil →
• GW
  GAD Wasim

  PCVRR
  Voir le profil →
• KD
  KOSTOVA Desislava

  PCVRR
  Voir le profil →
• GAD Wasim
  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. The reporting obligations referred to in Articles 87 to 91 are fulfilled
  Masqué
• YOUSSEF Nermeen
  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.
  Masqué
• KOSTOVA Desislava
  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.
  Masqué
• ADEL Rojeh
  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.
  Masqué

• 3EC International a.s. — 14 certificats — Pharmaplast
• E C REP LIMITED — représente — Pharmaplast
• ADEL Rojeh — Pharmaplast
• GAD Wasim — Pharmaplast
• KOSTOVA Desislava — Pharmaplast