Vascular guide-catheter, single-use - UK MHRA Medical Device Registration
Vascular guide-catheter, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 200157. The device is manufactured by Reflow Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Medes 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.
Device Type
General Medical Device
Devices
Vascular guide-catheter, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Sep 7, 2024
Address
208 Avenida Fabricante, Suite 100
San Clemente,, California, United States
Created Date
Sep 4, 2024
Name
Medes Ltd.Relationship Type
Address
5 Beaumont Gate, Shenley Hil
Radlett, Herts, England, United Kingdom
Postcode: WD77AR
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