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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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Dropper Pumps — 6 UDI-DI variants, MDR (Aero Pump GmbH)

MD Atlas
Aero Pump GmbH

Data from EUDAMED, last updated May 23, 2026

Dropper Pumps

426242274AD001SP

6 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: Aero Pump GmbH

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 426242274AD001SP
Device name: Dropper Pumps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: Aero Pump GmbH
SRN: DE-MF-000034723
Country: Germany
Email: matthias.kaiser@aeropump.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01H59TCVAKBMN5R7WNM8M7DGQP

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

60042500MD04262422740193
AcDrop04262422740155
AcDrop04262422740186
AcDrop04262422740162
AcDrop04262422740001
AcDrop04262422740025