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 143745. The device is manufactured by TONTARRA Medizintechnik 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: 143745•Ref: 143745

Device Type

General Medical Device

Devices

Middle ear file/rasp

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 6, 2024

Manufacturer Information

Name

TONTARRA Medizintechnik GmbH

Address

Daimlerstraße 15

Wurmlingen, Germany

Created Date

Oct 14, 2021

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 TONTARRA Medizintechnik GmbH (10)

Other Products from Same Authorized Representative (10)

Middle ear file/rasp - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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