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.

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Polymeric spinal interbody fusion cage

MHRA Device ID: 171566•Ref: 171566

Device Type

General Medical Device

Devices

Polymeric spinal interbody fusion cage

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Jun 10, 2023

Manufacturer Information

Name

Mediox Orvosi Műszergyártó Kft.

Address

2473 Hrsz

Felsőtárkány, Hungary

Created Date

May 5, 2023

Authorized Representative

Name

HUA TENG LIMITED

Relationship Type

UK Responsible Person

Address

3 Glass Street, Hanley

Stoke On Trent, England, United Kingdom

Postcode: ST1 2ET

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Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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