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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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Soluscope CLN — 18 UDI-DI variants, MDR (Soluscope SAS)

MD Atlas
Soluscope SAS

Data from EUDAMED, last updated May 19, 2026

Soluscope CLN

359761SS0150C1LI8S

18 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 359761SS0150C1LI8S
Device name: Soluscope CLN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 21, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

18 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K360C3PEEF53B6T0BBZ9TW5Q

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

3160369S303597610640261
31603696E03597610640230
3160369UL03597610641329
3160369EO03597610640223
22057378T03597610622014
2205737GZ03597610537806
214773703597610224720
22057379C03597610621994
2205737E703597610250170
3114542BN03597610652028
3114542BM03597610652011
31144859B03597610621871
31144855503597610613968
2483444FG03597610439704
24834444403597610596469
24834448W03597610622038
2483444GZ03597610537820
22057374Z03597610593703