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Revision uncoated femoral stem prosthesis - UK MHRA Medical Device Registration

Revision uncoated femoral stem prosthesis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 75281. The device is manufactured by ADLER ORTHO SPA from Italy, classified as General Medical Device. The authorized representative in the UK is ADLER ORTHO UK 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.

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Revision uncoated femoral stem prosthesis
MHRA Device ID: 75281โ€ขRef: 75281

Device Type

General Medical Device

Devices

Revision uncoated femoral stem prosthesis

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Nov 6, 2024

Manufacturer Information

Address

Via dell'Innovazione 9

Cormano (MI), Italy

Created Date

Apr 22, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Castle Chambers, 43 Castle Street

Liverpool, England, United Kingdom

Postcode: L2 9TL

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