United Kingdom MHRA device registration 65142

Manual brachytherapy source, permanent implant

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

Registration details

Device ID: 65142
Date Registered: Jan 30, 2021
Last Updated: Dec 22, 2022

Device classification

Device Type: Active implantable device (Directive 90/385/EEC only)
Devices: Manual brachytherapy source, permanent implant
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

Manual brachytherapy source, permanent implantNov 26, 2024

Type: General Medical Device

Manufacturer: Quirem Medical B.V.

Device ID: 186774

Manual brachytherapy source, permanent implantNov 26, 2024

Type: Active Implantable Device

Manufacturer: Quirem Medical B.V.

Device ID: 75766

Manual brachytherapy source, permanent implantNov 26, 2024

Type: Active Implantable Device

Manufacturer: Eckert & Ziegler BEBIG GmbH

Device ID: 78189

Manual brachytherapy source, permanent implantAug 2, 2024

Type: General Medical Device

Manufacturer: Sirtex Medical Pty Ltd

Device ID: 198242

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

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

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143460

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

Noninvasive device battery chargerApr 5, 2022

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

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143459

Personal device holder, reusableApr 5, 2022

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

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143464

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

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

Other products from Sirtex Medical Pty Ltd

Additional devices registered by the same manufacturer

Vial radiation shieldAug 2, 2024

Type: General Medical Device

Device ID: 198244

Radiation shielding container, general-purposeAug 2, 2024

Type: General Medical Device

Device ID: 198246

Syringe radiation shieldAug 2, 2024

Type: General Medical Device

Device ID: 198243

Manual brachytherapy source, permanent implantAug 2, 2024

Type: General Medical Device

Device ID: 198242

General-purpose brachytherapy system applicator, manualAug 2, 2024

Type: General Medical Device

Device ID: 198245

Syringe radiation shieldJan 30, 2021

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

Device ID: 90580

General-purpose brachytherapy system applicator, manualJan 30, 2021

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

Device ID: 65143

Vial radiation shieldJan 30, 2021

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

Device ID: 90578

Radiation shielding container, general-purposeJan 30, 2021

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

Device ID: 90579

Other products from same authorized representative

Additional devices represented by Donawa Lifescience Ltd in the UK

Negative-pressure wound therapy system foam dressing, non-antimicrobialNov 26, 2024

Type: General Medical Device

Manufacturer: Medical Device srl

Device ID: 182177

Peritoneal/extracorporeal dialysis dressing procedure kitNov 26, 2024

Type: General Medical Device

Manufacturer: Medical Device srl

Device ID: 182175

Wearable percutaneous catheter/tube holderNov 26, 2024

Type: General Medical Device

Manufacturer: Medical Device srl

Device ID: 182179

Laparoscopic insufflatorNov 26, 2024

Type: General Medical Device

Manufacturer: Lexion Medical

Device ID: 95086

Surgical instrument handle, non-torque-limitingNov 26, 2024

Type: General Medical Device

Manufacturer: Rhein83 Srl

Device ID: 91169

Cardiopulmonary stress exercise monitoring systemNov 26, 2024

Type: General Medical Device

Manufacturer: Cosmed Srl

Device ID: 67452

Metabolic measurement trolleyNov 26, 2024

Type: General Medical Device

Manufacturer: Cosmed Srl

Device ID: 178352

Catheter orifice occluderNov 26, 2024

Type: General Medical Device

Manufacturer: Delta Med SpA

Device ID: 88431

Double-ended bag access spikeNov 26, 2024

Type: General Medical Device

Manufacturer: Delta Med SpA

Device ID: 97204

Central venous catheterization kit, long-termNov 26, 2024

Type: General Medical Device

Manufacturer: Medical Device srl

Device ID: 182178

About this record

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.

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