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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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FRANCY O3 — 2 UDI-DI variants, MDR (TT Med s.r.l.)

MD Atlas
TT Med s.r.l.

Data from EUDAMED, last updated May 30, 2026

FRANCY O3

805368783FRANCYOWP

2 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: TT Med s.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805368783FRANCYOWP
Device name: FRANCY O3
Device model: FRANCY O3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: TT Med s.r.l.
SRN: IT-MF-000033862
Country: Italy
Email: info@ttmed.it
Phone: +0390721797301

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GVG3HRMM58TFFMM73D8B3NHN

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

FRANCY O308053687830103
FRANCY O4, POLTRONA O.R.L.08053687830110