Manual brachytherapy source, permanent implant - UK MHRA Medical Device Registration
Manual brachytherapy source, permanent implant is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 65142. The device is manufactured by Sirtex Medical Pty Ltd from Australia, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Donawa Lifescience Ltd.
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
Active implantable device (Directive 90/385/EEC only)
Devices
Manual brachytherapy source, permanent implant
Type
Active implantable Medical device
Date Registered
Jan 30, 2021
Last Updated
Dec 22, 2022
Address
Shop 6 207 Pacific Highway
St Leonards, Australia
Created Date
Jan 30, 2021
Relationship Type
Address
Aviation Business Park Enterprise Close
Christchurch, England, United Kingdom
Postcode: BH23 6NX
Manual brachytherapy source, permanent implant
Type: General Medical Device
Manufacturer: Quirem Medical B.V.
Manual brachytherapy source, permanent implant
Type: Active Implantable Device
Manufacturer: Quirem Medical B.V.
Manual brachytherapy source, permanent implant
Type: Active Implantable Device
Manufacturer: Eckert & Ziegler BEBIG GmbH
Manual brachytherapy source, permanent implant
Type: General Medical Device
Manufacturer: Sirtex Medical Pty Ltd
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
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Manual brachytherapy source, permanent implant
Type: General Medical Device
Registered: Aug 2, 2024
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Registered: Aug 2, 2024
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Registered: Jan 30, 2021
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Type: Active implantable device (Directive 90/385/EEC only)
Registered: Jan 30, 2021
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Registered: Jan 30, 2021
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