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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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AURYX 90 CA 72-4 Reagent Kit — 1 UDI-DI variant, IVDD

MD Atlas
PZ CORMAY Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

AURYX 90 CA 72-4 Reagent Kit

B-05907514600465

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — General

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Manufacturer: PZ CORMAY Spółka Akcyjna

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: B-05907514600465
Device name: AURYX 90 CA 72-4 Reagent Kit
Device model: AURYX 90 CA 72-4 Reagent Kit
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Version date: Jul 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: PZ CORMAY Spółka Akcyjna
SRN: PL-MF-000023053
Country: Poland
Email: regulatory_affairs@cormay.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01K10DB0VH94VYNWGNCMJSHDJY

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

AURYX 90 CA 72-4 Reagent Kit05907514600465