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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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Paediatric dosing device — 5 UDI-DI variants, MDR

MD Atlas
Effectum Medical AG

Data from EUDAMED, last updated May 23, 2026

Paediatric dosing device

764025502TD00849

5 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: Effectum Medical AG

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 764025502TD00849
Device name: Paediatric dosing device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 9, 2023

Manufacturer & authorised representative

Manufacturer

Name: Effectum Medical AG
SRN: CH-MF-000012474
Country: Switzerland
Email: info@effectummedical.com
Phone: +41 77 493 72 72

Authorised representative

Name: Emergo Europe B.V.
SRN: NL-AR-000000116
Country: Netherlands
Phone: +31 70 345 8570

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HA1SGHT1S9RY90X7965XYNC6

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

008.001.00107640255020410
008.001.00207640255020427
008.001.00307640255020632
008.001.00407640255020649
008.001.00507640255021004