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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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JUPITER — 6 UDI-DI variants, MDR

MD Atlas
Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

JUPITER

590450765175013L4

6 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: Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590450765175013L4
Device name: —
Device model: JUPITER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.
SRN: PL-MF-000038261
Country: Poland
Email: biuro@technomex.pl
Phone: +48324010350

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01J55DAKK1VGEQ1XVPGBHTPCFY

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

1750130305904507651374
1750130505904507651886
1750130605904507652784
1750130405904507651961
1750130105904507651985
1750130205904507652333