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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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Trioderm® CARE Kryosprej na odstranění… — 2 UDI-DI variants, MDR

MD Atlas
AVEFLOR, a.s.

Data from EUDAMED, last updated May 23, 2026

Trioderm® CARE Kryosprej na odstranění bradavic

859401370Z28NQ

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: AVEFLOR, a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859401370Z28NQ
Device name: Trioderm® CARE Kryosprej na odstranění bradavic
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: AVEFLOR, a.s.
SRN: CZ-MF-000003103
Country: Czechia
Email: aveflor@aveflor.cz
Phone: +420 493 551 111

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HAVPCC4SC7JF12TP9Q5FH7ZG

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

Trioderm® CARE Warts Removal Cryospray08594013705073
Z2808594013703802