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EUDAMED last updated this device on May 22, 2024
590364150PHPKRPolaris HP M is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by ASTAR spółka z ograniczoną odpowiedzialnością. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05903641500654A-UL-AST-PHPM1PL-MF-000010564(01)05903641500654
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
3 warnings recorded — scroll inside the panel to see all entries.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Poland; available across 7 countries total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Aug 2, 2023 | Still on market |
| Denmark | Apr 19, 2024 | Still on market |
| EL | Aug 27, 2024 | Still on market |
| Hungary | Aug 27, 2024 | Still on market |
| Iceland | Aug 27, 2024 | Still on market |
| Lithuania | Aug 27, 2024 | Still on market |
| Romania | Aug 27, 2024 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z120615THERAPEUTIC LASERSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →590364150PMGKNOn the marketPhysioMG 825590364150PMGKNOn the marketPhysioMG 827590364150PMGKNOn the marketPolaris HP S590364150PHPKROn the marketReusable electrotherapy and electrostimulation electrodes 6x6cm590364150ELV2C3On the marketReusable electrotherapy and electrostimulation electrodes 7,5x9cm590364150ELV2C3On the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
HZ 1962094-1SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →