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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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Medicine Cup — 4 UDI-DI variants, MDR (Kellpo A/S)

MD Atlas
Kellpo A/S

Data from EUDAMED, last updated May 23, 2026

Medicine Cup

57450009331020M6

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: Kellpo A/S

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 57450009331020M6
Device name: Medicine Cup
Device model: 1010
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Kellpo A/S
SRN: DK-MF-000023184
Country: Denmark
Email: info@kellpo.dk

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJ412VQGSW8TRJFQRRNRH18F

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

101705745000933235
101905745000933259
101805745000933242
101605745000933228