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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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Lyophilized rabbit plasma — 2 UDI-DI variants, IVDR (bioMérieux SA)

MD Atlas
bioMérieux SA

Data from EUDAMED, last updated May 31, 2026

Lyophilized rabbit plasma

357302BUDI000489U8

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: bioMérieux SA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 357302BUDI000489U8
Device name: Lyophilized rabbit plasma
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: bioMérieux SA
SRN: FR-MF-000004436
Country: France
Email: media@biomerieux.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHW14AC3HQ5VVH0YD5MV50N

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

Lyophilized rabbit plasma03573026584061
Lyophilized rabbit plasma03573026584078