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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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Ceveron m series — 3 UDI-DI variants, IVDR

MD Atlas
Technoclone Herstellung von Diagnostika und Arzneimitteln GmbH

Data from EUDAMED, last updated May 31, 2026

Ceveron m series

912003686TCCevm00001HX

3 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Technoclone Herstellung von Diagnostika und Arzneimitteln GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 912003686TCCevm00001HX
Device name: Ceveron m series
Device model: Ceveron m series
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Technoclone Herstellung von Diagnostika und Arzneimitteln GmbH
SRN: AT-MF-000024115
Country: Austria
Email: regulatory@technoclone.com
Phone: +431863730

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSQQYPAPYRSYWWH8J3JNE67G

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

983002109120036863989
983002209120036863996
983002409120036864009