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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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Ortezy — 68 UDI-DI variants, MDR (Orthoguard Maciej Tomczuk)

MD Atlas
Orthoguard Maciej Tomczuk

Data from EUDAMED, last updated May 30, 2026

Ortezy

5903981322ortezyRM

68 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: Orthoguard Maciej Tomczuk

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5903981322ortezyRM
Device name: Ortezy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Orthoguard Maciej Tomczuk
SRN: PL-MF-000002247
Country: Poland
Email: info@orthoguard.pl
Phone: +48 664 269 146

Variants by status

UDI-DI variants

68 UDI-DI variants

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Applied filters

basicUdiUlid01FQKN2TBKZ2XPQ2KX9AHR6G5V

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

OG-WR00105903981322084
OG-WR00105903981322145
OG-WR00205903981322220
OG-WR00105903981322138
OG-WR00205903981322213
OG-WR00205903981322206
OG-WR00105903981322121
OG-WR00205903981322237
OG-WR00105903981322152
OG-AN00105903981322114
OG-AN00105903981322107
OG-AN00105903981322091
OG-WA00105903981322022
OG-WA00105903981322015
OG-WA00105903981322039
OG-WA00105903981322046
OG-WA00105903981322244
OG-WA00105903981322008

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