United Kingdom MHRA device registration 204819

Ambulatory insulin infusion pump software, patient-dosing

United Kingdom·General Medical Device·mySugr GmbH·Registered Nov 26, 2024

Registration details

Device ID: 204819
MHRA Reference Number: 204819
Date Registered: Nov 26, 2024
Last Updated: Nov 9, 2024

Device classification

Device Type: General Medical Device
Devices: Ambulatory insulin infusion pump software, patient-dosing
Type: Class IIb

Manufacturer

Name: mySugr GmbH
Address: Trattnerhof 1/5 OG
Vienna, Austria
Created Date: Nov 7, 2024

Authorized Representative

Name: Roche Diagnostics Limited
Relationship Type: UK Responsible Person
Address: Roche Diagnostics Limited Charles Avenue
Burgess Hill, West Sussex, United Kingdom
Postcode: RH15 9RY

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About this record

Ambulatory insulin infusion pump software, patient-dosing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204819. The device is manufactured by mySugr GmbH from Austria, classified as General Medical Device. The authorized representative in the UK is Roche Diagnostics 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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