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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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Operating Table — 5 UDI-DI variants, MDR (SternMed GmbH)

MD Atlas
SternMed GmbH

Data from EUDAMED, last updated May 23, 2026

Operating Table

42517308014L5

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: SternMed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42517308014L5
Device name: Operating Table
Device model: Onex 101 / Onex 102 / Onex 201 / Onex 202 / Onex 203
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 5, 2023

Manufacturer & authorised representative

Manufacturer

Name: SternMed GmbH
SRN: DE-MF-000015421
Country: Germany
Email: info@sternmed.de
Phone: +49 757 35978 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G0CFHYWRXZTNFWY4MGP10VR2

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

300100204251730800484
300100004251730800460
300100304251730800491
300105004251730800453
300100104251730800477