Impulse Biomedical (Pty) Ltd

• Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
  BelgiumContact the authority →

No certificates registered for this manufacturer.

Devices placed in 13 countries

• Austria1
• Belgium1
• Germany1
• Spain1
• France1
• Ireland1
• Iceland1
• Italy1
• Liechtenstein1
• Luxembourg1
• Netherlands1
• Poland1
• XI1

2 contacts identified

• AS
  AMEEN Saajida

  PRRC
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• AMEEN Saajida
  Ensuring conformity of medical devices with the quality management system (QMS) before product release, in compliance with the EU MDR. Ensuring that the technical file and the EU Declaration of Conformity are maintained and updated. Implementing and maintaining a post-market surveillance system in line with EU MDR Article 83. Ensure all reporting obligations (adverse events, recalls, vigilance) are fulfilled as per EU MDR Articles 87-91.
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• Easy Medical Device — represents — Impulse Biomedical
• AMEEN Saajida — Impulse Biomedical