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.

AMPICILLIN 2 (B) E110129 — 12 UDI-DI variants, IVDR

MD Atlas
BioMaxima Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

AMPICILLIN 2 (B) E110129

59026439BASTAMLA

12 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
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: 59026439BASTAMLA
Device name: AMPICILLIN 2 (B) E110129
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Jul 7, 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

basicUdiUlid01JZJ7Z2BVQAKS1Q2J87ZWENTX

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

E110129 (B)05902643900073
E191826 (W)05902643982529
E191826 (K)05902643979529
E110129 (K)05902643978072
E110129 (W)05902643981072
E110125 (W)05902643981089
E110122 (W)05902643981065
E110125 (K)05902643978089
E110122 (K)05902643978065
E110122 (B)05902643900066
E191826 (B)05902643901520
E110125 (B)05902643900080