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 136574. The device is manufactured by JIMY BROTHERS GROUP from Pakistan, classified as General Medical Device. The authorized representative in the UK is Spire Instrumentation Ltd.
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
Nov 10, 2024
Address
Street Saga Yard Torabad Daska Road
Sialkot, Pakistan
Created Date
Feb 16, 2022
Relationship Type
Address
533 Bordesley Green,
Birmingham, England, United Kingdom
Postcode: B9 5XH
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