Self-care monitoring/reporting software - UK MHRA Medical Device Registration
Self-care monitoring/reporting software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209392. The device is manufactured by Florio GmbH from Germany, 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 23, 2025
Name
Florio GmbHAddress
Wilhelm-Wagenfeld-Strasse 22
Munich, Bavaria, Germany
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Self-care monitoring/reporting software
Type: General Medical Device
Registered: Nov 26, 2024
Self-care monitoring/reporting software
Type: General Medical Device
Registered: Nov 26, 2024
Self-care monitoring/reporting software
Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024

