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.

Free Database

MHRA Registered

General Medical Device

🇬🇧

Self-care monitoring/reporting software

MHRA Device ID: 209392

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Jan 23, 2025

Manufacturer Information

Name

Florio GmbH

Address

Wilhelm-Wagenfeld-Strasse 22

Munich, Bavaria, Germany

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Other Products from Florio GmbH (5)

Self-care monitoring/reporting software - UK MHRA Medical Device Registration

Device Type

Type

Status

Date Registered

Name

Address

DJ Fang

Custom-made talus prosthesis

External orthopaedic fixation system, reusable

Bone nail guidewire, reusable

General-body orifice lubricant, non-sterile

External orthopaedic fixation frame calculation software

External orthopaedic fixation system, reusable

Bone nail driver

Bone nail end-cap

Absorbent underpad, non-antimicrobial, single-use

External orthopaedic fixation system, single-use

Self-care monitoring/reporting software

Self-care monitoring/reporting software

Self-care monitoring/reporting software

Clinical management support software

Clinical management support software