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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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CYTOfast Plus — 1 UDI-DI variant, IVDR (Hospitex International S.r.l.)

MD Atlas
Hospitex International S.r.l.

Data from EUDAMED, last updated May 31, 2026

CYTOfast Plus

805099910CYI001CB

1 UDI-DI variant

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: Hospitex International S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805099910CYI001CB
Device name: CYTOfast Plus
Device model: CYTOfast Plus
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Hospitex International S.r.l.
SRN: IT-MF-000041985
Country: Italy
Email: info@hospitex.com
Phone: +39 055 0135766

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JVS4EP733DGT5G1QF4ANTZ0T

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

CYTOfast Plus08050999100009