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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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Spring Mattresses — 33 UDI-DI variants, MDR (Tempur Sealy DACH GmbH)

MD Atlas
Tempur Sealy DACH GmbH

Data from EUDAMED, last updated May 23, 2026

Spring Mattresses

805415452MOLLEBL

33 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: Tempur Sealy DACH GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805415452MOLLEBL
Device name: —
Device model: Spring Mattresses
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Tempur Sealy DACH GmbH
SRN: DE-MF-000048469
Country: Germany
Email: info@sealy.it

Variants by status

UDI-DI variants

33 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KREAWJ2T3SR8HJCFH7YQ99H2

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

7000703508054154521265
7000704208054154521081
7000676308054154520947
7000676408054154520954
7000676508054154520961
7000676908054154521005
7000677208054154521036
7000678108054154520879

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