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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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SemiRimCombo — 15 UDI-DI variants, MDR (xeyez)

MD Atlas
xeyez

Data from EUDAMED, last updated May 31, 2026

SemiRimCombo

10089578SemiRimComboMH

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: xeyez

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 10089578SemiRimComboMH
Device name: SemiRimCombo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: xeyez
SRN: NL-MF-000053485
Country: Netherlands
Email: info@xeyez.nl

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KRNNTYVRVX06AKKF9TKA5SZV

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

SRC5308721586820999
SRC5208721586820982
SRC5008721586820968
SRC4908721586820951
SRC4508721586820913
SRC5408721586821002
SRC4708721586820937
SRC5808721586821040
SRC4808721586820944
SRC4608721586820920
SRC5108721586820975
SRC5708721586821033
SRC4408721586820906
SRC5608721586821026
SRC5508721586821019