Gastro-oesophageal antireflux extraluminal fundal implant - UK MHRA Medical Device Registration
Gastro-oesophageal antireflux extraluminal fundal implant is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 80365. The device is manufactured by Implantica CE Reflux Ltd from Malta, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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
General Medical Device
Devices
Gastro-oesophageal antireflux extraluminal fundal implant
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Feb 15, 2024
Address
Sir Temi Zammit Buildings, Malta Life Sciences Park
San Gwann, Malta
Created Date
May 12, 2021
Relationship Type
Address
Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP
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Gastro-oesophageal antireflux extraluminal fundal implant
Type: General Medical Device
Registered: Nov 26, 2024
Gastro-oesophageal antireflux extraluminal fundal implant
Type: General Medical Device
Registered: Nov 26, 2024
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