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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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Visiocyt Bladder — 2 UDI-DI variants, IVDR (VitaDX International)

MD Atlas
VitaDX International

Data from EUDAMED, last updated May 19, 2026

Visiocyt Bladder

377002199701AM

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: VitaDX International

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 377002199701AM
Device name: Visiocyt Bladder
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Special device type: refdata.special-ivd-device-type.software
Version date: Jul 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: VitaDX International
SRN: FR-MF-000001855
Country: France
Email: regulatory@vitadx.com
Phone: +33143214455

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J35HW8F591AYG3NQBPMQ2K72

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

Visocyt Bladder03770021997012
Visiocyt Bladder03770021997050