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 101240. 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.

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Analytical non-scalp cutaneous lead

MHRA Device ID: 101240•Ref: 101240

Device Type

General Medical Device

Devices

Analytical non-scalp cutaneous lead

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Aug 9, 2024

Manufacturer Information

Name

Timpel S.A.

Address

Rua José Leonardi 280, Bloco A Aeroporto

Pato Branco, Paraná, Brazil

Created Date

Aug 31, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Analytical non-scalp cutaneous lead - 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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Analytical non-scalp cutaneous lead

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