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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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PRX-T33 — 2 UDI-DI variants, MDR (WiQo S.p.A.)

MD Atlas
WiQo S.p.A.

Data from EUDAMED, last updated May 30, 2026

PRX-T33

805045050MG195109038L

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: WiQo S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805045050MG195109038L
Device name: PRX-T33
Device model: MG19510903
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 20, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01J0TQVZ55Z6K85GHFE44P626B

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

PFMDR00208050450500416
PFMDR00108050450500409