Cannula clamp - UK MHRA Medical Device Registration

Cannula clamp is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 151601. The device is manufactured by Abiomed, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) 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.

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Cannula clamp

MHRA Device ID: 151601•Ref: 151601

Device Type

General Medical Device

Devices

Cannula clamp

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Abiomed, Inc.

Address

22 Cherry Hill Drive

Danvers, Massachusetts, United States

Created Date

Jun 22, 2022

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Cannula clamp - UK MHRA Medical Device Registration

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Date Registered

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DJ Fang

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