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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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DSC 8000 — 8 UDI-DI variants, MDR (Soluscope SAS)

MD Atlas
Soluscope SAS

Data from EUDAMED, last updated May 19, 2026

DSC 8000

359761SS01561QEQBT

8 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: Soluscope SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 359761SS01561QEQBT
Device name: DSC 8000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Soluscope SAS
SRN: FR-MF-000011763
Country: France
Email: contact@anios.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K3RFD175KR87VDRJTGAMCDY6

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

SC8-1D-C03760138530424
SC8-1D-A03760138530400
SC8L-1D-C03760138530493
SC8L-2D-A03760138530509
SC8L-2D-C03760138530516
SC8-2D-A03760138530448
SC8-2D-C03760138530462
SC8R-1D-C03760138530851