Leica Biosystems Richmond, Inc

• Ministerie van Volksgezondheid, Welzijn en Sport
  NetherlandsContact the authority →

Devices placed in 32 countries

• Netherlands352
• Austria342
• Belgium342
• Bulgaria342
• Cyprus342
• Czechia342
• Germany342
• Denmark342
• Estonia342
• Finland342
• France342
• Croatia342
• Hungary342
• Ireland342
• Iceland342
• Liechtenstein342
• Lithuania342
• Luxembourg342
• Latvia342
• Malta342
• Norway342
• Poland342
• Romania342
• Sweden342
• Slovenia342
• Slovakia342
• XI342
• Spain298
• Greece298
• Italy298
• Portugal298
• Türkiye298

No certificates registered for this manufacturer.

5 contacts identified

• CH
  CHIRNEV Heloiza

  PRRC
  View profile →
• LM
  LEWIS Mica

  PRRC
  View profile →
• ST
  SWANSON Teresa

  PRRC
  View profile →
• LEWIS Mica
  • Ensuring the technical documentation and the EU Declaration of Conformity are drawn up and kept up-to-date; • Investigational devices contain a signed statement required of Annex XIV Section 4.1 that the device conforms to the general safety and performance requirements apart from the aspects covered by the performance study.
  Hidden
• CHIRNEV Heloiza
  • Ensuring the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; • Ensure the post-market surveillance obligations in Articles 10(9) and 78 are complied with; • All vigilance reporting obligations referenced in Articles 82 to 86 are fulfilled.
  Hidden

• AR Experts B.V. — represents — LBS Richmond
• CEpartner4U — represents — LBS Richmond
• CHIRNEV Heloiza — LBS Richmond
• LEWIS Mica — LBS Richmond
• SWANSON Teresa — LBS Richmond