Coronary angioplasty balloon catheter, basic - UK MHRA Medical Device Registration
Coronary angioplasty balloon catheter, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203412. The device is manufactured by Goodman Co., Ltd. from Japan, 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.
Device Type
General Medical Device
Devices
Coronary angioplasty balloon catheter, basic
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Apr 23, 2024
Address
5F KDX Nagoya Sakae Building, 4-5-3 Sakae Naka-ku
Nagoya,, Aichi, Japan
Created Date
Feb 10, 2022
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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