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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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AXESS DUO D1 — 18 UDI-DI variants, MDR (FIRN SARL)

MD Atlas
FIRN SARL

Data from EUDAMED, last updated May 19, 2026

AXESS DUO D1

376036522TABLESB7

18 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: FIRN SARL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376036522TABLESB7
Device name: AXESS DUO D1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: FIRN SARL
SRN: FR-MF-000015675
Country: France
Email: info@firn.fr
Phone: +33388598959

Variants by status

UDI-DI variants

18 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K3TFBB108MF5XQP3GNK24WDJ

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

AXESS DUO D103760365220297
AXESS DUO D203760365220280
AXESS TRIO T103760365220273
AXESS TRIO T303760365220266
LUXURY DUO03760365220143
LUXURY TRIO03760365220136
MODUL CIFO 103760365220181
MODUL CIFO 303760365220174
MODUL DUO D103760365220006
MODUL DUO D203760365220259
MODUL DUO D303760365220242
MODUL DUO XL03760365220235
MODUL EXCEL E103760365220228
MODUL EXCEL E303760365220211
MODUL QUATRO03760365220167
MODUL SAXO03760365220150
MODUL TRIO TS103760365220204
MODUL TRIO TS303760365220198