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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 139368. The device is manufactured by MarFlow AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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.

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Polymeric ureteral stent
MHRA Device ID: 139368โ€ขRef: 139368

Device Type

General Medical Device

Devices

Polymeric ureteral stent

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 4, 2023

Manufacturer Information

Address

Soodstrasse 57, 8134 Adliswil,

Zรผrich, Switzerland

Created Date

Mar 9, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

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