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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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Moskinto — 9 UDI-DI variants, MDR (Apaloo GmbH)

MD Atlas
Apaloo GmbH

Data from EUDAMED, last updated May 23, 2026

Moskinto

426031010101Z5

9 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: Apaloo GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426031010101Z5
Device name: Moskinto
Device model: 10101
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: Apaloo GmbH
SRN: DE-MF-000016970
Country: Germany
Email: info@apaloo.de
Phone: +4907464980282

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01FZT428CA04GFSNQGVH5A764W

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

Insect Protect Pansements Après Piqures03760015790767
1010104260310410548
1010304260522560819
10101-204260310411118
1010904260310411828
1010704260310411422
1010504260310412290
1010604260310411439
10107-104260310411743