Intracerebral cannula, nonimplantable, single-use - UK MHRA Medical Device Registration
Intracerebral cannula, nonimplantable, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 80160. The device is manufactured by Alpha Omega Engineering Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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
Intracerebral cannula, nonimplantable, single-use
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Address
Hamerkava St.6, Tsiporit Industrial Zone
Nof HaGalil (Nazareth Illit), Israel
Created Date
May 10, 2021
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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