AF Pharma Service Europe SL

1 contact identified

• DUGUINE Maria
  Ensuring that: The conformity of medical devices is checked in accordance with the QM system (before delivery) (Article 10(9)). The technical documentation is kept up to date (Article 10(4) and (6)). Market surveillance is performed in compliance with the EU regulations (Article 10(10)). The reporting obligations according to the EU regulations are met (Article 10(13)). For “investigational devices”, the statement according to Annex XV, Chapter 2 is issued.
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• Agencia Española de Medicamentos y Productos Sanitarios
  SpainContact the authority →

65 non-EU manufacturers

• Medequip Healthcare Solutions Pvt Ltd 🇮🇳 IN296 devices
• ORTHOTECH Co., Ltd 🇰🇷 KR124 devices
• Nasmed Diagnostic Private Limited 🇮🇳 IN119 devices
• DUSONS MEDICARE LLP 🇮🇳 IN114 devices
• WOOSAM MEDICAL CO., LTD. 🇰🇷 KR105 devices
• Medipak 🇺🇸 US97 devices
• Suavepie SAIC 🇦🇷 AR85 devices
• JC ORTHOHEAL PRIVATE LIMITED 🇮🇳 IN43 devices
• 🇵🇰 PK43 devices
• 🇮🇳 IN37 devices
• 🇰🇷 KR33 devices
• 🇺🇰 UK32 devices
• 🇺🇰 UK23 devices
• 🇮🇳 IN22 devices
• 🇹🇼 TW20 devices
• 🇵🇰 PK14 devices
• 🇺🇸 US14 devices
• 🇺🇸 US14 devices
• 🇰🇷 KR12 devices
• 🇰🇷 KR12 devices
• 🇨🇦 CA11 devices
• 🇦🇺 AU10 devices
• 🇨🇭 CH9 devices
• 🇺🇸 US9 devices

• Medequip Healthcare Solutions Pvt Ltd — represents — AF Pharma Service Europe SL
• ORTHOTECH Co., Ltd — represents — AF Pharma Service Europe SL
• — represents — AF Pharma Service Europe SL
• — represents — AF Pharma Service Europe SL
• — represents — AF Pharma Service Europe SL
• — represents — AF Pharma Service Europe SL
• — represents — AF Pharma Service Europe SL
• — represents — AF Pharma Service Europe SL