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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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Foam & Memory Foam Mattresses — 42 UDI-DI variants, MDR

MD Atlas
BRENTAFLEX SRL SOCIETÀ BENEFIT

Data from EUDAMED, last updated May 31, 2026

Foam & Memory Foam Mattresses

805233441MTR0016E

42 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: BRENTAFLEX SRL SOCIETÀ BENEFIT

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805233441MTR0016E
Device name: Foam & Memory Foam Mattresses
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: BRENTAFLEX SRL SOCIETÀ BENEFIT
SRN: IT-MF-000029029
Country: Italy
Email: info@brentaflex.com
Phone: +39 049 5975300

Variants by status

UDI-DI variants

42 UDI-DI variants

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Applied filters

basicUdiUlid01K81084B0073S1FVDG3703EYW

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

No registered UDI-DI variants for this device family.