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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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Hielwigkussen — 3 UDI-DI variants, MDR (DecoCare)

MD Atlas
DecoCare

Data from EUDAMED, last updated May 30, 2026

Hielwigkussen

87209382652365YN

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: DecoCare

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87209382652365YN
Device name: Hielwigkussen
Device model: 2365 (75 x 48 x 2-10 cm)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: DecoCare
SRN: NL-MF-000015695
Country: Netherlands
Email: m.kluitmans@decocare.nl

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GVJA3TQZX7NP871MXQEC0TYP

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

232608720938265334
236508720938265051
236608720938265099