Cardiac ablation laser system beam guide-catheter - UK MHRA Medical Device Registration
Cardiac ablation laser system beam guide-catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 78001. The device is manufactured by CARDIOFOCUS INC from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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Device Type
General Medical Device
Devices
Cardiac ablation laser system beam guide-catheter
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Apr 27, 2024
Name
CARDIOFOCUS INCAddress
500 NICKERSON RD Suite 500-200
Marlborough, United States
Created Date
Apr 29, 2021
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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