Gastro-urological guidewire, single-use - UK MHRA Medical Device Registration
Gastro-urological guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209221. The device is manufactured by MarFlow AG from Switzerland, 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
Jan 22, 2025
Name
MarFlow AGAddress
Soodstrasse 57, 8134 Adliswil,
Zรผrich, Switzerland
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