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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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BASTONE CANADESE LEGA LEGGERA — 4 UDI-DI variants, MDR

MD Atlas
ALICE MEDICAL EXPORT SRL

Data from EUDAMED, last updated May 30, 2026

BASTONE CANADESE LEGA LEGGERA

80599161802058D

4 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: ALICE MEDICAL EXPORT SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80599161802058D
Device name: —
Device model: BASTONE CANADESE LEGA LEGGERA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: ALICE MEDICAL EXPORT SRL
SRN: IT-MF-000036718
Country: Italy
Email: ame@alicemedicalexport.com
Phone: +39 3 483 94 4942

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H90NN6TDEG7HQBYT0YYC940R

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

AM1810308059916180674
AM1810208059916180667
AM1810008059916180643
AM1810108059916180650