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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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Trattamento Crioterapico Verruche 50ml — 8 UDI-DI variants, MDR

MD Atlas
Sixtem Life Srl

Data from EUDAMED, last updated May 30, 2026

Trattamento Crioterapico Verruche 50ml

803277984VERRUCRYOEE

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Sixtem Life Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803277984VERRUCRYOEE
Device name: Trattamento Crioterapico Verruche 50ml
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: Sixtem Life Srl
SRN: IT-MF-000022977
Country: Italy
Email: info@sixtemlife.it
Phone: +390574572547

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJQTZB25A5XW094PW16BWEWX

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

VER600108032779841081
EXCILOR08032779841005
VER130208032779841012
VER180108032779841050
VER180208032779841067
VER000108032779840404
VER150108032779841036
VER140108032779841029