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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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Brucella Broth — 9 UDI-DI variants, IVDR (BioMaxima Spółka Akcyjna)

MD Atlas
BioMaxima Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

Brucella Broth

59026439ASBRBRNF

9 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: BioMaxima Spółka Akcyjna

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 59026439ASBRBRNF
Device name: Brucella Broth
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: BioMaxima Spółka Akcyjna
SRN: PL-MF-000039473
Country: Poland
Email: info@biomaxima.com
Phone: +48 81 440 83 71

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K8TNC7QPQF49VVTBK6XESEDG

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

Brucella Broth05902643914391
Brucella Broth05902643984899
PS 137- 50005902643904392
PW 3296S05902643941793
PW 329405902643938809
PW 329305902643941205
PW 3294S05902643941786
PW 3293S05902643941212
PW 329605902643941229