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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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Mikro-Applikatoren — 17 UDI-DI variants, MDR (Zantomed GmbH)

MD Atlas
Zantomed GmbH

Data from EUDAMED, last updated May 23, 2026

Mikro-Applikatoren

4260044630024X

17 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: Zantomed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4260044630024X
Device name: Mikro-Applikatoren
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 22, 2021

Manufacturer & authorised representative

Manufacturer

Name: Zantomed GmbH
SRN: DE-MF-000009550
Country: Germany
Email: j.brencic@zantomed.de
Phone: +49 203 60799812

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01FQH6S76ZRW2QCWM2TQX5GSYX

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

10303404260044630298
10303504260044630359
10303604260044630328
25294804260044630472
25294904260044630519
25295004260044630496
11135604260044630113
11750504260044630205
11135504260044630083
11135704260044630144
11752204260044630267
11751604260044630236
11748404260044630175
PP 90404260044630625
PP 90204260044630564
PP 90104260044630533
PP 90304260044630595