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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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Compressiekoussen — 16 UDI-DI variants, MDR (SolvaCare B.V.)

MD Atlas
SolvaCare B.V.

Data from EUDAMED, last updated May 30, 2026

Compressiekoussen

87184692SOLVAKOUSFV

16 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: SolvaCare B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87184692SOLVAKOUSFV
Device name: Compressiekoussen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: SolvaCare B.V.
SRN: NL-MF-000013820
Country: Netherlands
Email: info@solvacare.com

Variants by status

UDI-DI variants

16 UDI-DI variants

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Applied filters

basicUdiUlid01JKD73T3Q62E7YVED7GT75YHW

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

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21101408718469200047
21101308718469200030
21101208718469200023
21104408718469200849
21104308718469200832
21104208718469200825
21104108718469200818
21102108718469200214
21102408718469200245
21102308718469200238
21102208718469200221
21103408718469200344
21103308718469200337
21103208718469200320
21103108718469200313