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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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Rhino Cart — 6 UDI-DI variants, MDR (Medical Cart Company KFT)

MD Atlas
Medical Cart Company KFT

Data from EUDAMED, last updated May 24, 2026

Rhino Cart

5999861919RHINO00001BS

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: Medical Cart Company KFT

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5999861919RHINO00001BS
Device name: Rhino Cart
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 14, 2024

Manufacturer & authorised representative

Manufacturer

Name: Medical Cart Company KFT
SRN: HU-MF-000024286
Country: Hungary
Email: info@medicalcartcompany.hu
Phone: 003623920790

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01HXVRKMGD75FQA5QMEBZ6H17Q

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

Avalanche Plus Cart05999861919024
Avalanche SI Cart05999861919055
Rhino 0 Cart 1 Piece05999861919246
Rhino 1 Cart with Display Mount 1 Piece05999861919048
Rhino 4 Cart with Display Mount and KeyboardTray 1 Piece05999861919239
Rhino Accessorised Cart 1 Piece05999861919321