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.

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Polymeric ureteral stent

MHRA Device ID: 183999•Ref: 183999

Device Type

General Medical Device

Devices

Polymeric ureteral stent

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 30, 2024

Manufacturer Information

Name

Hunan Reborn Medical Science and Technology Development Co., Ltd

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

Authorized Representative

Name

MedPath Limited

Relationship Type

UK Responsible Person

Address

27 Old Gloucester Street

London, England, United Kingdom

Postcode: WC1N 3AX

DJ Fang

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Other Products from Hunan Reborn Medical Science and Technology Development Co., Ltd (5)

Other Products from Same Authorized Representative (10)

Polymeric ureteral stent - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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