018679921

CLARVIN

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March 30, 2022

Trademark Summary

The trademark application CLARVIN was filed by Clarvin AB, a corporation established under the laws of the Kingdom of Sweden (the "Applicant"). The application was published for oppositions on June 16, 2022, and still open for oppositions.

The application was filed in Swedish (English was selected as the second language).

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Goods And Services

• The mark was filed in class 35 with following description of goods:
  
  1. Business assistance, management and administrative services
  2. Business consultancy and advisory services
  3. Marketing research
  4. Business analysis and information services, and market research
  5. Evaluation of business opportunities
  6. Business consultancy and advisory services, in relation to the following fields: Technical medical devices
  7. Provision of commercial and business contact information
  8. Corporate advisory services, in relation to the following fields: Market establishment and Market surveillance
  9. Business representative services
  10. Nominee services, in relation to the following fields: Market establishment and Market surveillance
  11. Nominee services, namely a local retail representative
  12. Consultancy relating to corporate quality assurance in the field of management systems, management audit, internal audit, supplier audit and financial controls
  13. Computerised database management and data processing in the field of medical engineering and devices
  14. Business analysis, research and information services.
• The mark was filed in class 42 with following description of goods:
  
  1. Science and technology services
  2. Natural science services
  3. Testing, authentication and quality control
  4. Product quality evaluation
  5. Testing, analysis and evaluation of the goods of others for the purpose of certification
  6. Clinical investigation services
  7. Clinical research and testing services in the field of medical equipment and devices
  8. Services, in relation to the following fileds: Clinical research and testing in the field of technical medical devices
  9. Product development consultation in the fields of medical products and devices
  10. Providing advice, in relation to the following fileds: Product development in the field of medical preparations
  11. Providing advice, in relation to the following fileds: Product development in the field of technical medical devices
  12. Scientific services relating to the planning and conducting of clinical studies and research in the fields of medical equipment and devices
  13. Advisory services, in relation to the following fileds: Quality assurance in the field of research and product development
  14. Quality assurance consultancy
  15. Quality management and quality assurance in the field of the development of medical products and devices and technical medical devices
  16. Quality management and quality assurance of medical products and devices and technical medical devices.
• The mark was filed in class 44 with following description of goods:
  
  1. Medical services
  2. Medical evaluation services
  3. Advisory services relating to medical apparatus and instruments
  4. Advising, in relation to the following goods: Technical medical devices
  5. Consultancy and information services relating to medical products
  6. Consultancy and information relating to medical technology goods.
• The mark was filed in class 45 with following description of goods:
  
  1. Legal services
  2. Advisory services relating to regulatory affairs
  3. Advisory services relating to regulatory affairs, in relation to the following fields: Medical equipment and devices and technical medical devices
  4. Reviewing standards and practices to assure compliance with laws and regulations
  5. Regulatory compliance auditing
  6. Information services relating to manufacturing standards
  7. Information services relating to trading standards
  8. Consultancy relating to regulatory compliance and validation procedures
  9. Consultancy relating to compliance with regulatory requirements
  10. Consultancy relating to regulatory compliance and validation procedures to ensure compliance with clinical trials in the field of medical equipment and devices
  11. Consultancy relating to regulatory compliance and validation procedures to ensure compliance in the field of medical equipment and devices
  12. Providing information on government regulatory bodies' examination and approval processes for medical equipment and devices
  13. Consultancy relating to regulatory compliance and validation procedures to ensure compliance relating to technical medical devices
  14. Providing of information on government regulatory bodies' examination and approval processes for technical medical devices
  15. Nominee services relating to regulatory compliance and adherence to regulatory requirements.