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 214354. The device is manufactured by Cordis US Corp. from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class IIa
Status
Date Registered
Mar 29, 2025
Name
Cordis US Corp.Address
14201 North West 60th Avenue
Miami Lakes, Florida, United States
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