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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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Fox-Lyz 10× (50 ml) — 2 UDI-DI variants, IVDR

MD Atlas
I.T.A.-Intertact s.r.o.

Data from EUDAMED, last updated May 23, 2026

Fox-Lyz 10× (50 ml)

859421827FXL05000WQ

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: I.T.A.-Intertact s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859421827FXL05000WQ
Device name: Fox-Lyz 10× (50 ml)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: I.T.A.-Intertact s.r.o.
SRN: CZ-MF-000003664
Country: Czechia
Email: nemec.m@ita-intertact.com
Phone: +420 224 810 196

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRNPZY2HKQEHAB452T3Z239X

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

100-05000-0608594218270031
100-05000-0508594218270024