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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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SPARTA LP — 30 UDI-DI variants, MDR (Ortoiberica S.L.)

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

SPARTA LP

8431184P1920000Y9

30 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: Ortoiberica S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431184P1920000Y9
Device name: SPARTA LP
Device model: P-1920-000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Ortoiberica S.L.
SRN: ES-MF-000025780
Country: Spain
Email: welcome@ortoiberica.es
Phone: +34985794800

Variants by status

UDI-DI variants

30 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HAMGHBTDZ8PJ51H76NQZBY4D

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

P-1925-02608431184250264
P-1925-02708431184250271
P-1925-02908431184250295
P-1921-02608431184210268
P-1922-02608431184220267

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