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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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plusoptiX 12 — 4 UDI-DI variants, MDR (Plusoptix GmbH)

MD Atlas
Plusoptix GmbH

Data from EUDAMED, last updated May 23, 2026

plusoptiX 12

426018451x12HA

4 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: Plusoptix GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426018451x12HA
Device name: plusoptiX 12
Device model: A12C, A12R, S12C, S12R
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 19, 2022

Manufacturer & authorised representative

Manufacturer

Name: Plusoptix GmbH
SRN: DE-MF-000006138
Country: Germany
Email: c.schmidt@plusoptix.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G0EJY76TMH251APF7AT1FXV0

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

A12C04260184512119
A12R04260184513116
S12C04260184512218
S12R04260184513215