Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Orteza kończyny dolnej — 8 UDI-DI variants, MDR

MD Atlas
Orthoguard Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Orteza kończyny dolnej

5905957672OGWK00QM

8 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 Sp. z o.o.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5905957672OGWK00QM
Device name: Orteza kończyny dolnej
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Orthoguard Sp. z o.o.
SRN: PL-MF-000050865
Country: Poland
Email: info@orthoguard.pl
Phone: +48664269146

Variants by status

UDI-DI variants

8 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KFQ4H2PYEKK5MBTPC2P2SEEM

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

L05905957672162
M05905957672155
S05905957672148
XL05905957672179
L05905957672209
M05905957672193
S05905957672186
XL05905957672216