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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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CUILLERE 5ml — 4 UDI-DI variants, MDR (Rovipharm)

MD Atlas
Rovipharm

Data from EUDAMED, last updated May 19, 2026

CUILLERE 5ml

3666663CUDOS3E

4 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: Rovipharm

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 3666663CUDOS3E
Device name: CUILLERE 5ml
Device model: CUILLERE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Rovipharm
SRN: FR-MF-000000673
Country: France
Email: regulatory@sgh-medical.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GYAECMCQ59YCMTC7HYRJG4CR

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

26500021 03760337568099
26500981 03760337568198
2650097103760337568044
2650010103760337568051