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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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Latex Mattresses — 3 UDI-DI variants, MDR (ITALBED SRL)

MD Atlas
ITALBED SRL

Data from EUDAMED, last updated May 30, 2026

Latex Mattresses

805762260MTR004DL

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: ITALBED SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805762260MTR004DL
Device name: Latex Mattresses
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: ITALBED SRL
SRN: IT-MF-000047490
Country: Italy
Email: amministrazioneitalbed@permaflex.it
Phone: +390516935500

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KC95PK640158824ME3A77T9B

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

DG2PREXXXYYYS0Z08057622601544
DG2PREXXXYYYS0Z08057622601551
DG2PREXXXYYYS0Z08057622601568