Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

ILUX LF D15 — 1 UDI-DI variant, MDD (Mectronic Medicale srl)

MD Atlas
Mectronic Medicale srl

Data from EUDAMED, last updated May 31, 2026

ILUX LF D15

B-08051499971564

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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-08051499971564
Device name: ILUX LF D15
Device model: ILUX LF D15
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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KRGTHTMVXQ51SBQESGS7VD95

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

10LFD1508051499971564