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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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PUNTALE GOMMA — 2 UDI-DI variants, MDR (ALICE MEDICAL EXPORT SRL)

MD Atlas
ALICE MEDICAL EXPORT SRL

Data from EUDAMED, last updated May 30, 2026

PUNTALE GOMMA

80599161802068F

2 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: 80599161802068F
Device name: —
Device model: PUNTALE GOMMA
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

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H90S5KDH6P8AD8SEHNJEQAXE

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

AM18A0108059916180681
AM18A0208059916180698