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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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Opaska dziana — 6 UDI-DI variants, MDR

MD Atlas
Andrzej Bugajski ,,DALPEX" Przedsiębiorstwo Produkcyjno-Handlowe

Data from EUDAMED, last updated May 31, 2026

Opaska dziana

590198609001FM

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Andrzej Bugajski ,,DALPEX" Przedsiębiorstwo Produkcyjno-Handlowe

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590198609001FM
Device name: Opaska dziana
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Andrzej Bugajski ,,DALPEX" Przedsiębiorstwo Produkcyjno-Handlowe
SRN: PL-MF-000036903
Country: Poland
Email: biuro@dalpex.pl
Phone: +48 787 979 761

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KMQ9YNC1DEZPZKAPFWDV8QBP

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

OPD_4x10_APTEO05908312470625
OPD_4x15_APTEO05908312470632
OPD_4x5_APTEO05908312470618
OPD_4x10_3MMM05901986093060
OPD_4x15_3MMM05901986093077
OPD_4x5_3MMM05901986093053