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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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ABX Minotrol Retic — 5 UDI-DI variants, IVDR (HORIBA ABX SAS)

MD Atlas
HORIBA ABX SAS

Data from EUDAMED, last updated May 19, 2026

ABX Minotrol Retic

361023minotrol_reticB2

5 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: HORIBA ABX SAS

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Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 361023minotrol_reticB2
Device name: ABX Minotrol Retic
Device model: 2072201, 2072202, 1300136023, 1300136026, 1300136029
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Jun 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: HORIBA ABX SAS
SRN: FR-MF-000000320
Country: France
Email: caroline.ferrer@horiba.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JX010HAZ9K63E9ZT8Y4VBY0T

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

2072201, 2072202, 1300136023, 1300136026, 130013602903610230008898
130013602303610230009710
ABX Minotrol Retic03610230009734
207220203610230008904
130013602603610230009727