Middle ear file/rasp - UK MHRA Medical Device Registration
Middle ear file/rasp is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 153197. The device is manufactured by FENTEX medical GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL UK 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
Middle ear file/rasp
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jan 16, 2024
Address
take-off GewerbePark 2
Neuhausen ob Eck, Baden-Wรผrttemberg, Germany
Created Date
Jul 22, 2022
Relationship Type
Address
2 St Andrews Place
Lewes, East Sussex, England, United Kingdom
Postcode: BN7 1UP
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