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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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REALICA SEDATION — 3 UDI-DI variants, MDR (VALIAMO SRL)

MD Atlas
VALIAMO SRL

Data from EUDAMED, last updated May 31, 2026

REALICA SEDATION

805329545REALICAVRJ5

3 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: VALIAMO SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805329545REALICAVRJ5
Device name: REALICA SEDATION
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Jun 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: VALIAMO SRL
SRN: IT-MF-000014882
Country: Italy
Email: info@valiamo.it
Phone: +39 0 4231916688

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JYRMDKFE73AY6B5R2K62BFJV

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

REALICA BABE08053295450021
REALICA DENTAL SEDATION08053295450014
REALICA SEDATION08053295450007