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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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Dosing cup — 7 UDI-DI variants, MDR (Rovipharm)

MD Atlas
Rovipharm

Data from EUDAMED, last updated May 19, 2026

Dosing cup

3666663GOBELET35

7 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 functionAdministers medicine

Identity & classification

Basic UDI-DI: 3666663GOBELET35
Device name: Dosing cup
Device model: GOB60.5 ; GOB30 ; GOB13
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 14, 2024

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HPKZ2W4MANJPBPE5XDEK9XJ5

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

26105201 03760337568075
2610504103760337568211
26900011 03760337568167
2610503103760337568136
2610510103760337568228
2690002103760337568242
26103061 03760337568150