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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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VX22 — 3 UDI-DI variants, MDR (Luneau Technology Operations)

MD Atlas
Luneau Technology Operations

Data from EUDAMED, last updated May 19, 2026

VX22

13664188000152LL

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: Luneau Technology Operations

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 13664188000152LL
Device name: VX22
Device model: VX22
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Luneau Technology Operations
SRN: FR-MF-000009091
Country: France
Email: contact@visionix.com
Phone: +33 2 32 98 91 32

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KR1ZMH3J9T1EJ59R04GX3BK0

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

VX22-CP03664188000251
VX22-LP03664188000244
VX22-NP03664188000237