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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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ORTO PRO — 12 UDI-DI variants, MDR

MD Atlas
IRR spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

ORTO PRO

59076842ORTOPROEC

12 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: IRR spółka z ograniczoną odpowiedzialnością

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59076842ORTOPROEC
Device name: —
Device model: ORTO PRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: IRR spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000024038
Country: Poland
Email: biuro@corbby.com.pl

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJSA85F9AWJMGV7SHCWBDC8X

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

6400C05907684264009
6391C05907684263910
6393C05907684263934
6390C05907684263903
6395C05907684263958
6397C05907684263972
6398C05907684263989
6396C05907684263965
6389C05907684263897
6399C05907684263996
6392C05907684263927
6394C05907684263941