Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration
Polymeric spinal interbody fusion cage is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 171566. The device is manufactured by Mediox Orvosi Műszergyártó Kft. from Hungary, classified as General Medical Device. The authorized representative in the UK is HUA TENG LIMITED.
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
Polymeric spinal interbody fusion cage
Type
Class IIb
Date Registered
Apr 11, 2024
Last Updated
Jun 10, 2023
Name
HUA TENG LIMITEDRelationship Type
Address
3 Glass Street, Hanley
Stoke On Trent, England, United Kingdom
Postcode: ST1 2ET
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