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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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MESA ÒPTICA / Electric ophthalmic… — 10 UDI-DI variants, MDR

MD Atlas
ANTONI CARLES S.A.

Data from EUDAMED, last updated May 23, 2026

MESA ÒPTICA / Electric ophthalmic instrument table

8436566191TABGE

10 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: ANTONI CARLES S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8436566191TABGE
Device name: MESA ÒPTICA / Electric ophthalmic instrument table
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: ANTONI CARLES S.A.
SRN: ES-MF-000001010
Country: Spain
Email: ancar@ancar-online.com
Phone: +34 93 754 07 97

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FY6J6XKVRAH8C100Q2W3W2KP

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

42-000008208436566192361
122909408436566192385
122910308436566192439
42-000008008436566192453
42-000008108436566192460
120130908436566192484
120131308436566192569
800062708436566192859
120150008436566192125
42-000001008436566192248