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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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Trypticasein Soy LAB-AGAR™ (TSA) — 10 UDI-DI variants, IVDR

MD Atlas
BioMaxima Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

Trypticasein Soy LAB-AGAR™ (TSA)

59026439ASTSAQ9

10 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: 59026439ASTSAQ9
Device name: Trypticasein Soy LAB-AGAR™ (TSA)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 5, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9A1BMMND71APRKZ023C1674

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

PS 22- 5KG05902643924925
BT 700205902643951334
BT 5000.0205902643949515
PP 118005902643930537
BT 5000.0105902643949508
PP 011805902643931855
PS 22- 50005902643909670
Trypticasein Soy LAB-AGAR™ (TSA)05902643990173
Trypticasein Soy LAB-AGAR™ (TSA)05902643919679
PW 306205902643940338