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.

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Middle ear file/rasp

MHRA Device ID: 153197•Ref: 153197

Device Type

General Medical Device

Devices

Middle ear file/rasp

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jan 16, 2024

Manufacturer Information

Name

FENTEX medical GmbH

Address

take-off GewerbePark 2

Neuhausen ob Eck, Baden-Württemberg, Germany

Created Date

Jul 22, 2022

Authorized Representative

Name

MEDAGENT INTERNATIONAL UK LIMITED

Relationship Type

UK Responsible Person

Address

2 St Andrews Place

Lewes, East Sussex, England, United Kingdom

Postcode: BN7 1UP

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Other Products from FENTEX medical GmbH (10)

Other Products from Same Authorized Representative (10)

Middle ear file/rasp - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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