Prism Medical UK

No certificates registered for this manufacturer.

Devices placed in 10 countries

• XI497
• Ireland496
• Czechia7
• Netherlands6
• Italy5
• Denmark3
• Spain1
• Finland1
• France1
• Iceland1

2 contacts identified

• MI
  MORRIS Ian

  PRRC
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• MORRIS Ian
  The conformity of medical devices is checked in accordance with the QM system (before delivery) (Article 10(9)) Post Market surveillance is performed in compliance with the EU regulations (Article 10(10)). The technical documentation is kept up to date (Article 10(4) and (6)). 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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• Health Products Regulatory Authority, Medical Devices Department
  IrelandContact the authority →

• Evolution Healthcare Ltd — represents — N/A
• MORRIS Ian — N/A