Stryker Medical

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

Devices placed in 32 countries

• Ireland171
• Netherlands171
• Luxembourg169
• Malta169
• Austria166
• Germany166
• Belgium165
• Italy162
• Sweden162
• Finland159
• Iceland158
• Spain157
• Denmark156
• Liechtenstein153
• France149
• Portugal141
• Estonia136
• Hungary135
• Latvia134
• Czechia126
• Slovenia125
• Slovakia124
• Lithuania118
• Poland118
• Romania117
• Norway115
• Croatia106
• Cyprus11
• Greece10
• Türkiye3
• XI3
• Bulgaria1

18 contacts identified

• BZ
  BAKER Zachary

  PRRC
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• DZ
  DEVECI Zisan

  PRRC
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• ER
  EWING Rob

  PRRC
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• HB
  HALTEH Breskella

  PRRC
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• LB
  LIEDKE Brent

  PRRC
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• LT
  LOPEZ Tara

  PRRC
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• MJ
  MACK John

  PRRC
• MT
  PRRC
• MD
  PRRC
• PN
  PRRC
• PD
  PRRC
• MURALI Divya
  Ensure the technical documentation and the EU declaration of conformity are drawn up and kept up to date in accordance with the EU Medical Device Regulations. Ensure the reporting of serious incidents and field safety corrective actions in accordance with the EU Medical Device Regulations.
  Hidden
• LIEDKE Brent
  Ensure post-market surveillance obligations are complied with in accordance with the EU Medical Device Regulations.
  Hidden
• MAY Tom
  Check the conformity of devices in accordance with the quality management system under which the device is manufactured before the device is released into the market. (Article 15.3(a)).
  Hidden
• DEVECI Zisan
  Check the conformity of devices in accordance with the quality management system under which the device is manufactured before the device is released into the market. (Article 15.3(a)).
  Hidden
• BAKER Zachary
  Ensure that clinical investigations are carried out in accordance with the EU Medical Device Regulations
  Hidden
• MACK John
  Ensure the clinical investigations are carried out in accordance with the EU Medical Device Regulations
  Hidden
• PAUL Dita
  Ensure the technical documentation and the EU declaration of conformity are drawn up and kept up to date in accordance with the EU Medical Device Regulations. Ensure post-market surveillance obligations are complied with in accordance with the EU Medical Device Regulations Ensure the reporting of serious incidents and field safety corrective actions in accordance with the EU Medical Device Regulations.
  Hidden

• Stryker Medical — US-MF-000000542
• Stryker Medical — US-MF-000002456
• Stryker Medical — US-MF-000004430 · inactive
• — 1 certificate — Stryker Medical
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