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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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FLOWTENS ANKLE BRACE — 3 UDI-DI variants, MDR (Flowstim Technology)

MD Atlas
Flowstim Technology

Data from EUDAMED, last updated May 19, 2026

FLOWTENS ANKLE BRACE

3770025687FLO-02-108-R2V

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Flowstim Technology

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770025687FLO-02-108-R2V
Device name: FLOWTENS ANKLE BRACE
Device model: ANKLE BRACE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Flowstim Technology
SRN: FR-MF-000018490
Country: France
Email: contact@flowstim-technology.com
Phone: 0617981694

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JC5EXEWKD7KYTYV3QBTMJ0WV

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

FLOWTENS LEFT ANKLE BRACE03770025687032
FLOWTENS PATCH03770025687094
FLOWTENS RIGHT ANKLE BRACE03770025687025