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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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EOSIN-RAL 555 — 4 UDI-DI variants, IVDR (RAL Diagnostics)

MD Atlas
RAL Diagnostics

Data from EUDAMED, last updated May 19, 2026

EOSIN-RAL 555

376017719361640KS

4 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: RAL Diagnostics

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Device characteristics

Reagent

Identity & classification

Basic UDI-DI: 376017719361640KS
Device name: EOSIN-RAL 555
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: RAL Diagnostics
SRN: FR-MF-000007902
Country: France
Email: info@ral-diagnostics.fr
Phone: +33557960404

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KR19CTQKGY304PGYV4C98BFS

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

EOSIN-RAL 55503760177193079
EOSIN-RAL 55503760177193062
EOSIN-RAL 55503760177195783
EOSIN-RAL 55503760177193086