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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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StandardLine Manual — 6 UDI-DI variants, MDR (Ropox a/s)

MD Atlas
Ropox a/s

Data from EUDAMED, last updated May 23, 2026

StandardLine Manual

57075810017RC

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: Ropox a/s

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57075810017RC
Device name: StandardLine Manual
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ropox a/s
SRN: DK-MF-000020145
Country: Denmark
Email: info@ropox.dk

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKGSTTT5FPFCP6HJXT9HS398

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

40-14787-105707581016400
40-14786-105707581016394
40-14789-105707581016424
40-14788-105707581016417
40-14765-105707581015137
40-14760-105707581015120