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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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Laser therapy unit Polaris HP — 2 UDI-DI variants, MDR

MD Atlas
ASTAR spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Laser therapy unit Polaris HP

590364150PHPKR

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: ASTAR spółka z ograniczoną odpowiedzialnością

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590364150PHPKR
Device name: Laser therapy unit Polaris HP
Device model: S, M
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: ASTAR spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000010564
Country: Poland
Email: eudamed@astar.eu
Phone: +48338292440

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HYFV36WYHEBA0XV09K143HJ7

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

A-UL-AST-PHPM105903641500654
A-UL-AST-PHPS105903641500661