Arteriovenous fistula buttonhole cannulation guide - UK MHRA Medical Device Registration

Arteriovenous fistula buttonhole cannulation guide is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180404. The device is manufactured by Ultra for medical products (Ultramed) Co (U.M.I.C) S.A.E. from Egypt, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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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Arteriovenous fistula buttonhole cannulation guide

MHRA Device ID: 180404•Ref: 180404

Device Type

General Medical Device

Devices

Arteriovenous fistula buttonhole cannulation guide

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Aug 30, 2024

Manufacturer Information

Name

Ultra for medical products (Ultramed) Co (U.M.I.C) S.A.E.

Address

Part No. (304:310) & part no. (312) – Industrial Area, Arab El Awamer

Abnoub, Assiut , Egypt

Created Date

Oct 16, 2023

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Other Products from Ultra for medical products (Ultramed) Co (U.M.I.C) S.A.E. (10)

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Arteriovenous fistula buttonhole cannulation guide - UK MHRA Medical Device Registration

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Created Date

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