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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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Lunaris IO — 6 UDI-DI variants, MDR (Axiles Bionics BV)

MD Atlas
Axiles Bionics BV

Data from EUDAMED, last updated May 23, 2026

Lunaris IO

54040365PD00001TC

6 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: Axiles Bionics BV

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 54040365PD00001TC
Device name: Lunaris IO
Device model: Lunaris IO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Axiles Bionics BV
SRN: BE-MF-000025722
Country: Belgium
Email: claire@axilesbionics.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GHEWMDVDSCA31TPA6BNWKRXQ

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

LUNC4SXXZ05404036500131
LUNC2SXXZ05404036500117
LUNC6SXXZ05404036500155
LUNC7SXXZ05404036500162
LUNC5SXXZ05404036500148
LUNC3SXXZ05404036500124