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

MD Atlas
xeyez

Data from EUDAMED, last updated May 31, 2026

SemiRimVaria

10089578SemiRimVariaRJ

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: 10089578SemiRimVariaRJ
Device name: SemiRimVaria
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

basicUdiUlid01KRNQN4C362BS0HVXT548G7HJ

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

SRV4408721586821057
SRV5608721586821170
SRV4508721586821064
SRV5308721586821149
SRV5408721586821156
SRV4608721586821071
SRV5008721586821118
SRV4908721586821101
SRV5708721586821187
SRV5808721586821194
SRV4708721586821088
SRV5508721586821163
SRV5208721586821132
SRV4808721586821095
SRV5108721586821125