Polydioxanone/polyethylene suture - UK MHRA Medical Device Registration
Polydioxanone/polyethylene suture is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 74137. The device is manufactured by Theragenics Corporation from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is BXTAccelyon 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
Polydioxanone/polyethylene suture
Type
Active implantable Medical device
Date Registered
Apr 20, 2021
Last Updated
Dec 22, 2022
Address
5203 Bristol Industrial Way
Buford, Georgia, United States
Created Date
Apr 20, 2021
Name
BXTAccelyon LtdRelationship Type
Address
The Coach House Grenville Court Britwell Road
Burnham, Buckinghamshire, England, United Kingdom
Postcode: SL1 8DF
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Manufacturer: Theragenics Corporation
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Theragenics Corporation

