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 134146. The device is manufactured by Ackermann Instrumente 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: 134146•Ref: 134146

Device Type

General Medical Device

Devices

Fistula probe

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 16, 2024

Manufacturer Information

Name

Ackermann Instrumente GmbH

Address

Eisenbahnstr. 65-67

Rietheim-Weilheim , Baden-Württemberg , Germany

Created Date

Jul 5, 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

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Address

Created Date

Name

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Address

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