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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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ILUX LF V10 — 1 UDI-DI variant, MDD (Mectronic Medicale srl)

MD Atlas
Mectronic Medicale srl

Data from EUDAMED, last updated May 31, 2026

ILUX LF V10

B-08051499974121

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Mectronic Medicale srl

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Device characteristics

Active device

Legacy certificates

Certificate number: 1833/MDD
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. (0051)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-08051499974121
Device name: ILUX LF V10
Device model: ILUX LF V10
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 13, 2026

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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Applied filters

basicUdiUlid01KRGTZZPZ4K1D8QMWMZSA2HVY

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

10LFV1008051499974121