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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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Luchtwisseldruk matras — 7 UDI-DI variants, MDR

MD Atlas
Van der Mark Anti Decubitus Systemen

Data from EUDAMED, last updated May 30, 2026

Luchtwisseldruk matras

8720256271AD11208RW

7 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: Van der Mark Anti Decubitus Systemen

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8720256271AD11208RW
Device name: Luchtwisseldruk matras
Device model: Luchtwisseldruk matras
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: Van der Mark Anti Decubitus Systemen
SRN: NL-MF-000005763
Country: Netherlands
Email: info@ad-systemen.nl
Phone: +31186573585

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G65M31QS44RPCNB5RCXZGXR1

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

2020810508720256271031
20208105-21008720256271062
2020812008720256271048
112089408720256271024
1120894-21008720256271055
2020710008720256271017
112087508720256271000