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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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Kula łokciowa — 7 UDI-DI variants, MDR (Orthoguard Sp. z o.o.)

MD Atlas
Orthoguard Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

Kula łokciowa

5905957672OG-MO-AXI-ERG6Z

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: Orthoguard Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5905957672OG-MO-AXI-ERG6Z
Device name: Kula łokciowa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPXKC5WV34MJJ7RRSP644D3E

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-MO-AXI -ERG-BGE-UN05905957672285
OG-MO-AXI -ERG-BLK-UN05905957672254
OG-MO-AXI -ERG-RED-UN05905957672261
OG-MO-AXI -ERG-BLU-UN05905957672292
OG-MO-AXI-LNK-GRY-UN05905957672315
OG-MO-AXI -ERG-GRY-UN05905957672278
OG-MO-AXI-ERG-TRQ-UN05905957672308