Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

REAGENTI FISSAZIONE (ISTOLOGIA/CITOLOGI… — 7 UDI-DI variants, IVDR

MD Atlas
Pro-Eko Srl

Data from EUDAMED, last updated May 30, 2026

REAGENTI FISSAZIONE (ISTOLOGIA/CITOLOGIA)

805624938W010307059E

7 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 805624938W010307059E
Device name: REAGENTI FISSAZIONE (ISTOLOGIA/CITOLOGIA)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 2, 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

7 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01HK4Q36YE3ASH3TYPXJ9H27FK

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

IC002.25080562493800094
IC002.50080562493803996
IC20380562493802456
IC20480562493801602
IC02480562493803446
IC302.10080562493803200
IC302.50080562493802838