Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Columbia LAB-AGAR™ Base — 12 UDI-DI variants, IVDR

MD Atlas
BioMaxima Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

Columbia LAB-AGAR™ Base

59026439ASCOLMW

12 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 59026439ASCOLMW
Device name: Columbia LAB-AGAR™ Base
Device model: 100 g
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

12 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01K8TJ25PHGE0FSM0VP8GYJXMY

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

PP 024205902643930544
PP 002005902643929432
PP 119005902643929449
PP 021105902643929456
PD 03205902643931114
PS 06- 50005902643904996
BT 5011.0505902643946309
Columbia LAB-AGAR™ Base05902643985490
BT 5011.0205902643946293
PS 06- 5KG05902643924772
BT 5011.0105902643946286
Columbia LAB-AGAR™ Base05902643914995