Endocarts International Limited

• Health Products Regulatory Authority, Medical Devices Department
  IrelandContact the authority →

No certificates registered for this manufacturer.

Devices placed in 18 countries

• Spain61
• Ireland61
• Norway61
• Poland61
• Portugal61
• Belgium60
• Denmark60
• France60
• Greece60
• Italy60
• Finland4
• Czechia3
• Hungary2
• Lithuania2
• Latvia2
• Netherlands2
• Iceland1
• Sweden1

2 contacts identified

• AS
  PRRC
• ANGELL Stuart
  1) Verify that the conformity of the devices is appropriately checked in accordance with the QMS before a device is released. 2) Maintain and update the technical documentation and declaration of conformity 3) Review complaints reportability and submit incident report to CA/AR/NB, if applicable 4) Review and compile periodic post market surveillance report (PMS) 5) Review and update the clinical evaluation report (CER)
  Hidden

• Acorn Regulatory Consultancy Services Ltd — represents — Endocarts
• ANGELL Stuart — Endocarts