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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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Powiększalniki — 7 UDI-DI variants, MDR

MD Atlas
MIRACLE ROBERT BIEGAŃSKI MAŁGORZATA BAUER SPÓŁKA JAWNA

Data from EUDAMED, last updated May 30, 2026

Powiększalniki

59050686953POC5

7 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: MIRACLE ROBERT BIEGAŃSKI MAŁGORZATA BAUER SPÓŁKA JAWNA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59050686953POC5
Device name: Powiększalniki
Device model: Exigo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 29, 2024

Manufacturer & authorised representative

Manufacturer

Name: MIRACLE ROBERT BIEGAŃSKI MAŁGORZATA BAUER SPÓŁKA JAWNA
SRN: PL-MF-000040195
Country: Poland
Email: biuro@miracle.org.pl
Phone: +48 725 25 35 35

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01HQTR78M6F6C7KEEFQ8HNY7PY

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

POAD205905068695333
POE305905068695302
POE4U05905068695364
POPE505905068695340
POP105905068695326
POS305905068695319
POS4U05905068695357