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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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Fazer — 6 UDI-DI variants, MDR (Ludwig Artzt GmbH)

MD Atlas
Ludwig Artzt GmbH

Data from EUDAMED, last updated May 23, 2026

Fazer

426007163LA6001N3

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: Ludwig Artzt GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426007163LA6001N3
Device name: Fazer
Device model: Instrument Assisted Massage
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: Ludwig Artzt GmbH
SRN: DE-MF-000012141
Country: Germany
Email: info@artzt.eu
Phone: +49 6436 944930

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01H8166HA9NVMZRYJCK4E9NYPX

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

LA-701104260071636553
LA-701304260071636577
LA-701204260071636560
LA-701404260071636584
LA-701504260071639073
LA-701004260071638977