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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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Beam splitter — 5 UDI-DI variants, MDR (OPTOMIC ESPAÑA S.A)

MD Atlas
OPTOMIC ESPAÑA S.A

Data from EUDAMED, last updated May 23, 2026

Beam splitter

84360415804142Y

5 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: OPTOMIC ESPAÑA S.A

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 84360415804142Y
Device name: Beam splitter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: OPTOMIC ESPAÑA S.A
SRN: ES-MF-000003235
Country: Spain
Email: prrc@optomic.com
Phone: +34 91 804 44 44

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JC65NZTKF24SWQ4VC3MYG77G

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

7100328808436041580195
7100325508436041580188
7100361408436041580225
7100312808436041580171
7100331608436041580218