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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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ALCOMAX — 1 UDI-DI variant, MDR (XENODERM S.R.L.)

MD Atlas
XENODERM S.R.L.

Data from EUDAMED, last updated May 30, 2026

ALCOMAX

8056098091231DAL1001F3

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: XENODERM S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8056098091231DAL1001F3
Device name: ALCOMAX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: XENODERM S.R.L.
SRN: IT-MF-000031000
Country: Italy
Email: francesco.muollo@xenoderm.it
Phone: +39 0818568081

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01H4E1C7RZBHS2H6GAGDYJQ7FX

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

DLA100108056098091231