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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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Hektoen LAB-AGAR™ — 7 UDI-DI variants, IVDR (BioMaxima Spółka Akcyjna)

MD Atlas
BioMaxima Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

Hektoen LAB-AGAR™

59026439ASHEKTNP

7 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: 59026439ASHEKTNP
Device name: Hektoen LAB-AGAR™
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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K8TKFBF40SCD5R00GH6RKSA4

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

BT 5111.0105902643946842
PP 106005902643929753
BT 5111.0205902643946859
BT 5111.0505902643946866
PS 07- 50005902643905955
Hektoen LAB-AGAR™05902643915954
Hektoen LAB-AGAR™05902643924598