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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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Universal operating table RAMED — 12 UDI-DI variants, MDR

MD Atlas
RAMED Kopřivnice s.r.o.

Data from EUDAMED, last updated May 23, 2026

Universal operating table RAMED

859420869UOSWH

12 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: RAMED Kopřivnice s.r.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 859420869UOSWH
Device name: Universal operating table RAMED
Device model: UOS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: RAMED Kopřivnice s.r.o.
SRN: CZ-MF-000043587
Country: Czechia
Email: raska@ramed.cz
Phone: +420 602 731 912, +420 556 802 321

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJ6V7ECR100M5XAKQ99J5MFN

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

4200-0008594208690016
4300-0308594208690245
5300-0008594208690047
4300-0208594208690238
8300-0108594208690078
6300-0108594208690054
5300-0808594208690351
5200-0408594208690818
5300-0708594208690344
7300-0008594208690061
5200-0008594208690030
4300-0008594208690023