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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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Ophthalmic Table SE1 — 9 UDI-DI variants, MDR

MD Atlas
POLAND OPTICAL SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 30, 2026

Ophthalmic Table SE1

5905913529OPTTABLELE

9 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: POLAND OPTICAL SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5905913529OPTTABLELE
Device name: Ophthalmic Table SE1
Device model: Ophthalmic Table SE1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: POLAND OPTICAL SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000037042
Country: Poland
Email: sekretariat@po.pl
Phone: +48 33 851 36 30

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01HAP9KY52HVHQVZX7SN5WKGMP

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

Ophthalmic Table SE105905913529103
Ophthalmic Table SE1K05905913529127
Ophthalmic Table SE1OC05905913529219
Ophthalmic Table SE205905913529110
Ophthalmic Table SE2A05905913529165
Ophthalmic Table SE2K05905913529134
Ophthalmic Table SOCT105905913529141
Ophthalmic Table SOCT205905913529158
SW105905913529288