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.

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Intracerebral cannula, nonimplantable, single-use

MHRA Device ID: 80160•Ref: 80160

Device Type

General Medical Device

Devices

Intracerebral cannula, nonimplantable, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Alpha Omega Engineering Ltd.

Address

Hamerkava St.6, Tsiporit Industrial Zone

Nof HaGalil (Nazareth Illit), Israel

Created Date

May 10, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Other Products from Alpha Omega Engineering Ltd. (10)

Other Products from Same Authorized Representative (10)

Intracerebral cannula, nonimplantable, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Intracerebral cannula, nonimplantable, single-use

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