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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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LASERIX PRO — 3 UDI-DI variants, MDR (GN MED s.r.l.)

MD Atlas
GN MED s.r.l.

Data from EUDAMED, last updated May 31, 2026

LASERIX PRO

805432982Z1206153A

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: GN MED s.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805432982Z1206153A
Device name: LASERIX PRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: GN MED s.r.l.
SRN: IT-MF-000027922
Country: Italy
Email: surveillance@gnmed.it
Phone: +39 0542641837

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KAV1EV3XQ8YRWEXAPVBDSJDC

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

DOLORCLAST HIGH POWER LASER08054329820049
LASERIX PRO08054329820070
LASERIX PRO SMART08054329820384