Carl Zeiss Vision GmbH

• DE/CA37, Regierungspräsidium Stuttgart
  GermanyContact the authority →

Devices placed in 27 countries

• Germany13
• Austria5
• Belgium5
• Czechia5
• Spain5
• France5
• Greece5
• Hungary5
• Poland5
• Portugal5
• Romania5
• Slovakia5
• Denmark4
• Finland4
• Croatia4
• Ireland4
• Luxembourg4
• Netherlands4
• Sweden4
• Slovenia4
• Bulgaria3
• Italy3
• Estonia2
• Latvia2
• Cyprus1
• Lithuania1
• Malta1

4 contacts identified

• BD
  BECKERT Dr. Susanne

  PRRC
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• KN
  KHAYKINA Nadezda

  PRRC
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• KHAYKINA Nadezda
  The Person Responsible for Regulatory Compliance is responsible for ensuring compliance with the responsibilities set out in Article 15, acc. to Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices (MDR), Chapter II, Art. 15.
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• BECKERT Dr. Susanne
  Business Sector Vision Technology Solutions (BS VTS): - The technical documentation is drawn up and kept up to date. - The post-market surveillance obligations are compiled in accordance with Article 10. - The case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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• Carl Zeiss Vision GmbH — DE-MF-000006173
• Carl Zeiss Vision GmbH — DE-PR-000040411
• DQS Medizinprodukte GmbH — 1 certificate — Carl Zeiss Vision GmbH
• BECKERT Dr. Susanne — Carl Zeiss Vision GmbH
• KHAYKINA Nadezda — Carl Zeiss Vision GmbH