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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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Materac medyczny RUMBA — 11 UDI-DI variants, MDR

MD Atlas
Hilding Anders Polska Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

Materac medyczny RUMBA

5901595odlezynyGG

11 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: Hilding Anders Polska Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5901595odlezynyGG
Device name: Materac medyczny RUMBA
Device model: RUMBA VELUR 80x200
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: Hilding Anders Polska Sp. z o.o.
SRN: PL-MF-000032133
Country: Poland
Email: info.pl@hildinganders.com
Phone: +48 61 642 14 00

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H142M9EFFZY7R3BF6HNZ448H

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

G0B2A2D01605901595007342
G0B2A2D00805901595007243
G0B2A2C00805901595007106
G0B2A2C01605901595007205
G0B2A2C008N05901595007113
G0B2A1D01605901595007069
G0B2A1D00805901595006970
G0B2A1C01605901595006932
G0B2A1C00805901595006840
G0HAKF016005901595018454
G0HAKF008005901595018409