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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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ALIVIOVISCO — 13 UDI-DI variants, MDR (LIDERMED S.A.)

MD Atlas
LIDERMED S.A.

Data from EUDAMED, last updated May 23, 2026

ALIVIOVISCO

18426716ALIVI01KK

13 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: LIDERMED S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 18426716ALIVI01KK
Device name: ALIVIOVISCO
Device model: APÓSITOS PARA HERIDAS, LLAGAS Y ÚLCERAS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: LIDERMED S.A.
SRN: ES-MF-000004664
Country: Spain
Email: mario@lidermed.com
Phone: 663133901

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KNVH0AECNKZS0YCHK872JC34

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

011014008426716101404
011015108426716101510
011014208426716101428
011012008426716101206
011010508426716101053
011015208426716101527
011015408426716101541
011012208426716101220
011014508426716101459
011014708426716101473
011015508426716101558
011015308426716101534
011012108426716101213