AIR LIQUIDE MEDICAL SYSTEMS PRIVATE LIMITED

• Agence Nationale de Sécurité du Médicament et des Produits de Santé
  FranceContact the authority →

Devices placed in 1 country

• France2

2 contacts identified

• NR
  N R CHANDRA KUMAR

  PRRC
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• N R CHANDRA KUMAR
  As per the EU MDR 2017/745 Art.15, "Main responsibilities are followings:" - Conformity of the product device to the Medical Device Regulation and Quality Management System - Conformity of the Technical Documentation and EU Declaration of conformity - Compliance with Post-Market Surveillance (PMS) following Article 10(10) - Compliance with the Vigilance Reporting obligations (Article 87 to 91) - For Investigational devices: Issuance of a signed statement (Annex XV Chapter II Section 4.1)
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• TÜV SÜD Product Service GmbH — 1 certificate — AIR LIQUIDE MEDICAL SYSTEMS PVT LTD
• Air Liquide Medical Systems S.A. — represents — AIR LIQUIDE MEDICAL SYSTEMS PVT LTD
• N R CHANDRA KUMAR — AIR LIQUIDE MEDICAL SYSTEMS PVT LTD