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QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • Legit.Health Plus Version 1.1.0.0
    • Index
    • Overview and Device Description
    • Information provided by the Manufacturer
    • Design and Manufacturing Information
    • GSPR
    • Benefit-Risk Analysis and Risk Management
    • Product Verification and Validation
    • Design History File
    • Post-Market Surveillance
  • Legit.Health Plus Version 1.1.0.1
  • Licenses and accreditations
  • Applicable Standards and Regulations
  • Grants
  • Public tenders
  • Legit.Health Plus Version 1.1.0.0

Legit.Health Plus Version 1.1.0.0

📄️ Index

Index of Technical Documentation or Product File for Legit.Health Plus Version 1.1.0.0

🗃️ Overview and Device Description

3 items

🗃️ Information provided by the Manufacturer

3 items

🗃️ Design and Manufacturing Information

7 items

🗃️ GSPR

1 item

🗃️ Benefit-Risk Analysis and Risk Management

11 items

🗃️ Product Verification and Validation

4 items

🗃️ Design History File

5 items

🗃️ Post-Market Surveillance

4 items

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All the information contained in this QMS is confidential. The recipient agrees not to transmit or reproduce the information, neither by himself nor by third parties, through whichever means, without obtaining the prior written permission of Legit.Health (AI LABS GROUP S.L.)