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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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Ligorthese — 5 UDI-DI variants, MDR (Quattron Techniek BV)

MD Atlas
Quattron Techniek BV

Data from EUDAMED, last updated May 30, 2026

Ligorthese

87202993763LIG7B

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: Quattron Techniek BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87202993763LIG7B
Device name: Ligorthese
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2022

Manufacturer & authorised representative

Manufacturer

Name: Quattron Techniek BV
SRN: NL-MF-000001685
Country: Netherlands
Email: info@quattron.nl
Phone: 078-3030800

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G2VNRKZ23B3VR2GMAJD8MA84

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

Basis beenondersteuning08720299376335
C-ondersteuning08720299376342
Dynamic Support kussen model 1 08720299376304
Hoefijzerkussen08720299376311
J-ondersteuning08720299376328