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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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C50 — 14 UDI-DI variants, MDR (SOPRO)

MD Atlas
SOPRO

Data from EUDAMED, last updated May 19, 2026

C50

801337602782D0006CZ

14 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: SOPRO

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 801337602782D0006CZ
Device name: C50
Device model: S_C50_0001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: SOPRO
SRN: FR-MF-000000833
Country: France
Email: info@sopro.acteongroup.com
Phone: +33 4 42 98 01 01

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J290D55QY1B1MEQCMZ8JTFY2

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

S_C50_000103760278266894
S_C50_000203760278267020
S_C50_000303760278267723
S_C50_000403760278267730
C50 INTRAORAL CAMERA US03760278267587
C50 INTRAORAL CAMERA US DAYL03760278267594
S_950_000203760278260960
S_950_000803760278262797
S_950_000103760278260953
S_950_001103760278262827
S_950_000403760278260984
S_950_000303760278260977
S_950_001003760278262810
S_950_000903760278262803