Shoulder glenoid fossa prosthesis, prefabricated - UK MHRA Medical Device Registration
Shoulder glenoid fossa prosthesis, prefabricated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183240. The device is manufactured by Limacorporate S.p.A from Italy, classified as General Medical Device. The authorized representative in the UK is Lima Orthopaedics UK Ltd.
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Device Type
General Medical Device
Devices
Shoulder glenoid fossa prosthesis, prefabricated
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Sep 28, 2024
Address
via Nazionale 52
Villanova di San Daniele del Friuli, Italy
Created Date
Apr 27, 2021
Relationship Type
Address
The Pavillion Unit 1, Campus Five
Third Avenue, Letchworth Garden City, United Kingdom
Postcode: SG6 2JFL
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Polyethylene reverse shoulder prosthesis cup
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Type: General Medical Device
Manufacturer: Limacorporate S.p.A
Reverse shoulder prosthesis body
Type: General Medical Device
Manufacturer: Limacorporate S.p.A
Shoulder glenoid fossa prosthesis trial
Type: General Medical Device
Manufacturer: Limacorporate S.p.A
Shoulder humeral body prosthesis
Type: General Medical Device
Manufacturer: Limacorporate S.p.A
Sleeve femoral/tibial extension, coated
Type: General Medical Device
Manufacturer: Limacorporate S.p.A
Surgical implant template, reusable
Type: General Medical Device
Manufacturer: Limacorporate S.p.A
Surgical implant/trial-implant/sizer holder, reusable
Type: General Medical Device
Manufacturer: Limacorporate S.p.A
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Type: General Medical Device
Manufacturer: Limacorporate S.p.A

