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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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Rabbit coagulase plasma (lyophilized) — 2 UDI-DI variants, IVDR

MD Atlas
Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.

Data from EUDAMED, last updated May 30, 2026

Rabbit coagulase plasma (lyophilized)

590575374OSO002KD

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: Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 590575374OSO002KD
Device name: Rabbit coagulase plasma (lyophilized)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.
SRN: PL-MF-000042563
Country: Poland
Email: info@immunolab.com.pl
Phone: +48 58 781 44 91

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J3Q1TTCEQD2V3V240CENFQJ6

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

Rabbit coagulase plasma (lyophilized) - 2ml05905753743769
Rabbit coagulase plasma (lyophilized) - 5ml05905753743813