Analytical non-scalp cutaneous lead - UK MHRA Medical Device Registration
Analytical non-scalp cutaneous lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195612. The device is manufactured by Timpel S.A. from Brazil, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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
Analytical non-scalp cutaneous lead
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Aug 9, 2024
Name
Timpel S.A.Address
Rua Josรฉ Leonardi 280, Bloco A Aeroporto
Pato Branco, Paranรก, Brazil
Created Date
Aug 31, 2021
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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