Orthopaedic cement spacer - UK MHRA Medical Device Registration
Orthopaedic cement spacer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210392. The device is manufactured by Biomet Orthopaedics from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class IIb
Status
Date Registered
Feb 11, 2025
Address
56 East Bell Drive, P.O. Box 587
Warsaw, Indiana , United States
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Manufacturer: GE Medical Systems Information Technologies, Inc.
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Registered: Mar 6, 2025
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Type: General Medical Device
Registered: Mar 6, 2025
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Type: General Medical Device
Registered: Mar 6, 2025
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Type: General Medical Device
Registered: Mar 6, 2025
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Registered: Mar 6, 2025
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Type: General Medical Device
Registered: Feb 13, 2025

