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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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FYOX — 1 UDI-DI variant, MDD (WiQo S.p.A.)

MD Atlas
WiQo S.p.A.

Data from EUDAMED, last updated May 30, 2026

FYOX

B-08050450500539

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: WiQo S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-08050450500539
Device name: FYOX
Device model: MG20200518
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jun 21, 2024

Manufacturer & authorised representative

Manufacturer

Name: WiQo S.p.A.
SRN: IT-MF-000028707
Country: Italy
Email: info@wiqo.com
Phone: +39040360408

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01J0X5P2D7XMQHEHQ404B8FDZ3

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

PFFYX00108050450500539