Fistula probe - UK MHRA Medical Device Registration

Fistula probe is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 124259. The device is manufactured by RZ Medizintechnik 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.

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Fistula probe

MHRA Device ID: 124259•Ref: 124259

Device Type

General Medical Device

Devices

Fistula probe

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 13, 2024

Manufacturer Information

Name

RZ Medizintechnik GmbH

Address

Unter Hasseln 20

Tuttlingen , Germany

Created Date

Aug 27, 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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Fistula probe - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

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Address

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