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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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Rombusz kezelőágyak magasságállítással — 10 UDI-DI variants, MDR

MD Atlas
DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.

Data from EUDAMED, last updated May 24, 2026

Rombusz kezelőágyak magasságállítással

599957120RO00RS

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: DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 599957120RO00RS
Device name: Rombusz kezelőágyak magasságállítással
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 2023

Manufacturer & authorised representative

Manufacturer

Name: DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.
SRN: HU-MF-000003115
Country: Hungary
Email: dia-med@t-online.hu
Phone: +36209349740

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01HH4FYVK6GQH9EGRJCT1Z006B

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

RO1905999571200603
RO1505999571200054
RO1305999571200030
RO1205999571200023
RO2205999571200092
RO2305999571200108
RO1105999571200016
RO2105999571200085
RO1005999571200009
RO2005999571200078