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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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Sealy Generation — 15 UDI-DI variants, MDR (Tempur Sealy DACH GmbH)

MD Atlas
Tempur Sealy DACH GmbH

Data from EUDAMED, last updated May 23, 2026

Sealy Generation

805415452FOAMAV

15 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: 805415452FOAMAV
Device name: Sealy Generation
Device model: FOAM
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

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRE05TJSBDFHYY8XD5PTQDZJ

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

7000691608054154520367
7000691808054154520381
7000692108054154520411
7000692208054154520428
7000692308054154520435
7000692408054154520442
7000692508054154520459
7000693008054154520503
7000711208054154520527
7000693308054154520282
7000693508054154520305
7000693708054154520329
7000693808054154520336
7000694008054154520350
7000693208054154520275