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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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Manual hospital bed — 6 UDI-DI variants, MDR (TORUSCARE Sp. z o.o.)

MD Atlas
TORUSCARE Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Manual hospital bed

590218602MABED6Q

6 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: TORUSCARE Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590218602MABED6Q
Device name: —
Device model: Manual hospital bed
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: TORUSCARE Sp. z o.o.
SRN: PL-MF-000047801
Country: Poland
Email: karolina@toruscare.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JXVZ8MMY8DBHT4GG10Y5P4DJ

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

Manual hospital bed GRATO 205902186020146
Manual hospital bed GRATO 305902186020139
Manual hospital bed LAVA 205902186020115
Manual hospital bed LAVA 305902186020122
Manual hospital bed LAVA V305902186020108
Manual hospital bed LAVA W405902186020092