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 152471. The device is manufactured by Rebstock Instruments GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Delta Surgical 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
Fistula probe
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Mar 13, 2024
Relationship Type
Address
Unit 10 Evolution Lymedale Business Park
Newcastle under Lyme, Staffordshire, United Kingdom
Postcode: ST5 9QF
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