Bare-metal coronary artery stent - UK MHRA Medical Device Registration
Bare-metal coronary artery stent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 198984. The device is manufactured by Shockwave Medical, Inc. from United States, 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.
Device Type
System or Procedure Pack
Type
System or Procedure Pack
Status
Date Registered
Aug 16, 2024
Address
5403 Betsy Ross Drive
Santa Clara, California, United States
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Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
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Type: System or Procedure Pack
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Type: System or Procedure Pack
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General internal orthopaedic fixation system implantation kit
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
General internal orthopaedic fixation system implantation kit
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
General internal orthopaedic fixation system implantation kit
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
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Type: System or Procedure Pack
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Manufacturer: Cook Ireland Ltd
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Type: System or Procedure Pack
Registered: Sep 4, 2024
Ultrasonic lithotripsy system transducer, single-use
Type: General Medical Device
Registered: Sep 4, 2024
Ultrasound thrombolysis system control unit
Type: General Medical Device
Registered: Sep 4, 2024
Ultrasonic lithotripsy system transducer, single-use
Type: System or Procedure Pack
Registered: Sep 4, 2024
Ultrasonic lithotripsy system transducer, single-use
Type: System or Procedure Pack
Registered: Sep 4, 2024
Bare-metal coronary artery stent
Type: General Medical Device
Registered: Jul 31, 2024

