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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 SOFT — 12 UDI-DI variants, MDR

MD Atlas
IRR spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 31, 2026

ORTO SOFT

59076842ORTOSOFTTX

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: 59076842ORTOSOFTTX
Device name: —
Device model: ORTO SOFT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 21, 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

basicUdiUlid01KFFPB07H8A1R97C9HD4X46RH

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

1825C05907684218255
1830C05907684218309
1832C05907684218323
1822C05907684218224
1829C05907684218293
1831C05907684218316
1824C05907684218248
1827C05907684218279
1821C05907684218217
1826C05907684218262
1823C05907684218231
1828C05907684218286