United Kingdom MHRA device registration 90578

Vial radiation shield

United Kingdom·Active implantable device (Directive 90/385/EEC only)·Sirtex Medical Pty Ltd·Registered Jan 30, 2021

Registration details

Device ID: 90578
Date Registered: Jan 30, 2021
Last Updated: Dec 22, 2022

Device classification

Device Type: Active implantable device (Directive 90/385/EEC only)
Devices: Vial radiation shield
Type: Active implantable Medical device

Manufacturer

Name: Sirtex Medical Pty Ltd
Address: Shop 6 207 Pacific Highway
St Leonards, Australia
Created Date: Jan 30, 2021

Authorized Representative

Name: Donawa Lifescience Ltd
Relationship Type: UK Responsible Person
Address: Aviation Business Park Enterprise Close
Christchurch, England, United Kingdom
Postcode: BH23 6NX

Similar products

Devices with a matching generic name or device type registered with MHRA

Vial radiation shieldNov 26, 2024

Type: General Medical Device

Manufacturer: E-Z-EM INCORPORATED, a.d.b.a BRACCO DIAGNOSTICS INCORPORATED

Device ID: 141821

Vial radiation shieldNov 26, 2024

Type: General Medical Device

Manufacturer: Mirion Technologies (Capintec), Inc

Device ID: 190977

Vial radiation shieldAug 2, 2024

Type: General Medical Device

Manufacturer: Sirtex Medical Pty Ltd

Device ID: 198244

Vial radiation shieldApr 11, 2024

Type: General Medical Device

Manufacturer: Mirion Technologies (Capintec), Inc

Device ID: 187617

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system external electrodeApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143457

Noninvasive device battery chargerApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143459

Neurosurgical procedure kit, non-medicated, single-useApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143461

Personal device holder, reusableApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143464

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connectionApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143463

Soft-tissue/mesh anchor, non-bioabsorbableApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143460

Other products from Sirtex Medical Pty Ltd

Additional devices registered by the same manufacturer

General-purpose brachytherapy system applicator, manualAug 2, 2024

Type: General Medical Device

Device ID: 198245

Vial radiation shieldAug 2, 2024

Type: General Medical Device

Device ID: 198244

Syringe radiation shieldAug 2, 2024

Type: General Medical Device

Device ID: 198243

Radiation shielding container, general-purposeAug 2, 2024

Type: General Medical Device

Device ID: 198246

Manual brachytherapy source, permanent implantAug 2, 2024

Type: General Medical Device

Device ID: 198242

Syringe radiation shieldJan 30, 2021

Type: Active implantable device (Directive 90/385/EEC only)

Device ID: 90580

Radiation shielding container, general-purposeJan 30, 2021

Type: Active implantable device (Directive 90/385/EEC only)

Device ID: 90579

General-purpose brachytherapy system applicator, manualJan 30, 2021

Type: Active implantable device (Directive 90/385/EEC only)

Device ID: 65143

Manual brachytherapy source, permanent implantJan 30, 2021

Type: Active implantable device (Directive 90/385/EEC only)

Device ID: 65142

Other products from same authorized representative

Additional devices represented by Donawa Lifescience Ltd in the UK

Dental implant suprastructure, temporary, preformed, single-useNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 175795

Dental implantation drilling template guide-sleeveNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 163016

Dental precision attachment fitting/adjustment toolNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 127847

Dental prosthesis/implant abutment screwNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 127843

Dental prosthesis/implant abutment screwNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 175793

Surgical screwdriver, reusableNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 127844

Surgical torque wrench adaptorNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 127846

Intra-abdominal pressure measurement set, mechanicalNov 26, 2024

Type: General Medical Device

Manufacturer: Bioengineering Laboratories Srl

Device ID: 94593

Assisted reproduction embryo-assessment softwareNov 26, 2024

Type: General Medical Device

Manufacturer: Genea Biomedx Pty Ltd

Device ID: 100812

Dental implant suprastructure, temporary, preformed, single-useNov 26, 2024

Type: General Medical Device

Manufacturer: New Ancorvis Srl

Device ID: 175794

About this record

Vial radiation shield is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 90578. 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.

Free DatabasePowered by Pure Global AIMHRA RegisteredActive implantable device (Directive 90/385/EEC only)