Intra-aortic balloon catheter - UK MHRA Medical Device Registration
Intra-aortic balloon catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 87185. The device is manufactured by Datascope Corp. from United States, classified as General Medical Device. The authorized representative in the UK is Getinge Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, 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
General Medical Device
Devices
Intra-aortic balloon catheter
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Jul 23, 2024
Name
Getinge LimitedRelationship Type
Address
Unit 3 St Modwen Park Andressey Way Chaddesden
Derby, England, United Kingdom
Postcode: DE21 6YH
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Intra-aortic balloon catheter
Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Manufacturer: Datascope Corp.
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General-purpose drying cabinet
Type: General Medical Device
Manufacturer: Getinge Disinfection AB.
Hydrogen peroxide device sterilant
Type: General Medical Device
Manufacturer: Getinge Disinfection AB.
Medical device disinfection agent
Type: General Medical Device
Manufacturer: Getinge Disinfection AB.
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Type: General Medical Device
Manufacturer: Getinge Disinfection AB.
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Type: General Medical Device
Manufacturer: Getinge Disinfection AB.
Surgical instrument washer/disinfector (chemical/thermal)
Type: General Medical Device
Manufacturer: Getinge Disinfection AB.
Cardiac/peripheral vascular guidewire, single-use
Type: General Medical Device
Manufacturer: Datascope Corp.

