United Kingdom MHRA device registration 212361
Patient health record information system application software
Registration details
- Device ID
- 212361
- Status
- DREGIY
- Date Registered
- Mar 5, 2025
Device classification
- Device Type
- System or Procedure Pack
- Type
- System or Procedure Pack
Manufacturer
- Name
- RioMed Ltd
- Address
- 18 East Links, Chandlers FordEastleigh, Hampshire, England, United Kingdom
Similar products
Devices with a matching generic name or device type registered with MHRA
Instrument tray, reusableN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 141176
General internal orthopaedic fixation system implantation kitN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 79093
External orthopaedic fixation system, single-useN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 123523
Hard-tissue ultrasonic surgical systemN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 141186
General internal orthopaedic fixation system implantation kitN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 127332
General internal orthopaedic fixation system implantation kitN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 127333
General internal orthopaedic fixation system implantation kitN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 79092
Posterior-chamber intraocular lens, pseudophakicN/A
Type: System or Procedure Pack
Manufacturer: Caregroup Sight Solution Private Limited
Device ID: 176567
External orthopaedic fixation system, single-useN/A
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
Device ID: 160344
Tracheostomy kit, single-useN/A
Type: System or Procedure Pack
Manufacturer: Cook Ireland Ltd
Device ID: 176487
About this record
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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Free DatabasePowered by Pure Global AIMHRA RegisteredSystem or Procedure Pack