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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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XCE 12 blue — 3 UDI-DI variants, IVDR (MetaSystems Probes GmbH)

MD Atlas
MetaSystems Probes GmbH

Data from EUDAMED, last updated May 23, 2026

XCE 12 blue

42513158D-0812IVDJ8

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class C

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: MetaSystems Probes GmbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 42513158D-0812IVDJ8
Device name: XCE 12 blue
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Nov 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: MetaSystems Probes GmbH
SRN: DE-MF-000006315
Country: Germany
Email: info@metasystems-probes.com
Phone: +49 6205 29276-0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6ZAERMVD7F1DC1W18H9F4NZ

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

D-0812-050-BL04251315813106
D-0812-050-FI04251315813113
D-0812-050-OR04251315813120