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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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Coatron® A Series — 3 UDI-DI variants, IVDR

MD Atlas
TECO Medical Instruments, Production + Trading GmbH

Data from EUDAMED, last updated May 23, 2026

Coatron® A Series

426018278CAX809Z8

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: TECO Medical Instruments, Production + Trading GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 426018278CAX809Z8
Device name: Coatron® A Series
Device model: Coatron A generic product group
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: TECO Medical Instruments, Production + Trading GmbH
SRN: DE-MF-000022642
Country: Germany
Email: info@teco-medical.com
Phone: +49 8773 707800

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GR8R69F403566KCXVDW8P7T4

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

80 900 0004260182780909
80 920 0004260182780954
80 920 6004260182781005