Polymeric ureteral stent - UK MHRA Medical Device Registration
Polymeric ureteral stent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183999. The device is manufactured by Hunan Reborn Medical Science and Technology Development Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is MedPath 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
Polymeric ureteral stent
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 30, 2024
Address
Building B8 and B9, No.959, Tianyi Great Road, Xinmajingu Industrial Zone, Gaoxin District
Zhuzhou City, Hunan Province, China
Created Date
Dec 27, 2023
Name
MedPath LimitedRelationship Type
Address
27 Old Gloucester Street
London, England, United Kingdom
Postcode: WC1N 3AX
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