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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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Measuring cup — 3 UDI-DI variants, MDR (Serres Oy)

MD Atlas
Serres Oy

Data from EUDAMED, last updated May 23, 2026

Measuring cup

6418685SBS102K

3 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: Serres Oy

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Device characteristics

Measuring function

Legacy certificates

Certificate number: FI22/00000016
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: SGS FIMKO OY (0598)
Validity: Oct 25, 2025 → Oct 24, 2030

Identity & classification

Basic UDI-DI: 6418685SBS102K
Device name: Measuring cup
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: Serres Oy
SRN: FI-MF-000004504
Country: Finland
Email: quality@serres.com
Phone: +358 20 746 4400

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GR3ZEC2YEAR0TMWEEHBXR91K

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

5725706418685257017
57025706418685062642
57257-906418685023414