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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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SOLUZIONI COLORANTI (ISTOLOGIA/CITOLOGI… — 2 UDI-DI variants, IVDR

MD Atlas
Pro-Eko Srl

Data from EUDAMED, last updated May 30, 2026

SOLUZIONI COLORANTI (ISTOLOGIA/CITOLOGIA) KIT

805624938W01030708KLU

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: Pro-Eko Srl

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 805624938W01030708KLU
Device name: SOLUZIONI COLORANTI (ISTOLOGIA/CITOLOGIA) KIT
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: Pro-Eko Srl
SRN: IT-MF-000030078
Country: Italy
Email: info@proekosrl.com
Phone: +390875678657

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HKSSQK090ZMNKCSQW00AY9BZ

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

IC40180562493801770
IC40080562493802692