Patient health record information system application software - UK MHRA Medical Device Registration
Patient health record information system application software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 212361. The device is manufactured by RioMed Ltd from England, United Kingdom, classified as System or Procedure Pack.
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Device Type
System or Procedure Pack
Type
System or Procedure Pack
Status
Date Registered
Mar 5, 2025
Name
RioMed LtdAddress
18 East Links, Chandlers Ford
Eastleigh, Hampshire, England, United Kingdom
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