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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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Rollbord Professional Standard — 4 UDI-DI variants, MDR

MD Atlas
Samarit Medical AG

Data from EUDAMED, last updated May 23, 2026

Rollbord Professional Standard

764014446RbPro44020003Y

4 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: Samarit Medical AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764014446RbPro44020003Y
Device name: Rollbord Professional Standard
Device model: Professional
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 10, 2021

Manufacturer & authorised representative

Manufacturer

Name: Samarit Medical AG
SRN: CH-MF-000016280
Country: Switzerland
Email: info@samarit.com
Phone: +41 44 918 10 11

Authorised representative

Name: Samarit Medical Produkt GmbH
SRN: DE-AR-000014694
Country: Germany
Phone: +41 44 918 1011

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FM5GTJ0WP32R98KHN9Y2WZFN

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

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