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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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ACCESSORI PER DEAMBULATORE — 10 UDI-DI variants, MDR

MD Atlas
ALICE MEDICAL EXPORT SRL

Data from EUDAMED, last updated May 30, 2026

ACCESSORI PER DEAMBULATORE

805991618020389

10 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: 805991618020389
Device name: —
Device model: ACCESSORI PER DEAMBULATORE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 10, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H7FTMPYYW8DT0J2CB1ZF61DM

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

AM1800408059916180407
AM1800308059916180384
AM1801G08059916180612
AM1801A08059916180551
AM1801C08059916180575
AM1801B08059916180568
AM1801D08059916180582
AM1801E08059916180599
AM1801F08059916180605
AM18003T08059916180391