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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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IXYON XP ULTRA — 1 UDI-DI variant, MDR (Mectronic Medicale srl)

MD Atlas
Mectronic Medicale srl

Data from EUDAMED, last updated May 30, 2026

IXYON XP ULTRA

8051499971IXUG2

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Mectronic Medicale srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8051499971IXUG2
Device name: IXYON XP ULTRA
Device model: IXYON XP ULTRA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Sep 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Mectronic Medicale srl
SRN: IT-MF-000040989
Country: Italy
Email: info@mecmedix.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01K4VSJ26H2WS5XYNEEXYG0DG1

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

10IXUED050X08051499973926