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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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Medical table — 30 UDI-DI variants, MDR (CX Engineering sp. z o. o.)

MD Atlas
CX Engineering sp. z o. o.

Data from EUDAMED, last updated May 30, 2026

Medical table

59048157OphthTableTAVO84

30 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: CX Engineering sp. z o. o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59048157OphthTableTAVO84
Device name: Medical table
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: CX Engineering sp. z o. o.
SRN: PL-MF-000009247
Country: Poland
Email: regulatory.affairs@cxe.pl

Variants by status

UDI-DI variants

30 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JHPY0QRCZTR39BMM948Z2XW9

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

Electrical table Teburu_FF, TL version, 120-230V05904815701396
Electrical table Teburu_SSC_VX, 120V/230V05904815700191
Electrical table Teburu-MVS4.2, 100-240V, 4 wheels05904815701174
000000-2746-44505904815701327
7723020405904815700757

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