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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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Fotel do badań i zabiegów — 3 UDI-DI variants, MDR

MD Atlas
MEDEN-INMED SP. Z O.O.

Data from EUDAMED, last updated May 31, 2026

Fotel do badań i zabiegów

590368480M002BB

3 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: MEDEN-INMED SP. Z O.O.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590368480M002BB
Device name: Fotel do badań i zabiegów
Device model: MARS / WENUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDEN-INMED SP. Z O.O.
SRN: PL-MF-000001670
Country: Poland
Email: eudamed@meden.com.pl
Phone: 94 344 90 73 (w. 273)

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRXHGZM6B8QBWN4W251WYM9B

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

MARS05903684809806
MARS05903684809776
WENUS05903684809790