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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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M5Sc — 3 UDI-DI variants, MDR (Parallel Design SAS)

MD Atlas
Parallel Design SAS

Data from EUDAMED, last updated May 19, 2026

M5Sc

8406821BUG00112GQ

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Parallel Design SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8406821BUG00112GQ
Device name: M5Sc
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: Parallel Design SAS
SRN: FR-MF-000001806
Country: France
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GPB6TW1XP7SW9VYG1V6QZF5R

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

M5Sc-D00840682111966
571848200195278076632
5718483 00840682117883