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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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ANTI BED-SORE FOAM MATTRESS — 2 UDI-DI variants, MDR (M Prekyba UAB)

MD Atlas
M Prekyba UAB

Data from EUDAMED, last updated May 30, 2026

ANTI BED-SORE FOAM MATTRESS

477905414ORTONZ

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: M Prekyba UAB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 477905414ORTONZ
Device name: ANTI BED-SORE FOAM MATTRESS
Device model: ORTO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: M Prekyba UAB
SRN: LT-MF-000022623
Country: Lithuania
Email: info@mprekyba.lt
Phone: +37069889208

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J2XAZWM6SHJRAJE7HHRXNBXZ

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

ORTO04779054140159
ORTO04779054140166