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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 Hightec — 5 UDI-DI variants, MDR (Samarit Medical AG)

MD Atlas
Samarit Medical AG

Data from EUDAMED, last updated May 23, 2026

Rollbord Hightec

764014446RbHT4400000LF

5 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: 764014446RbHT4400000LF
Device name: Rollbord Hightec
Device model: Hightec
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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FM5DHKP2EKAWMRPKS38NX3XB

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

Rollbord Hightec Mini-Gyn07640144460037
Rollbord Hightec MRI/CT/AMBU07640144460051
Rollbord Hightec Surgiboard07640144460044
Rollbord Hightec ICU / Bariatric07640144460020
Rollbord Hightec Standard07640144460013