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PAWEŁ PINKOWSKI PPHU "ALGA"

Poland PL-MF-000046938 Last updated 17 Sep 2026

Devices
0
Registries
EUDAMED
FDA recalls
0

Catalogue0

No devices listed yet from this manufacturer.

About

A manufacturer of hygiene products PPHU ALGA PAWEŁ PINKOWSKI has over 20 years of experience in the manufacture of toilet paper, paper towels, ZZ and other similar products. Contact us to get a detailed offer.

Translated from the manufacturer's own website. Source

What PAWEŁ PINKOWSKI PPHU "ALGA" makes

The company produces medical-grade wipes, including standard and impregnated varieties, designed for single-use hygiene applications in clinical and healthcare settings.

These products fall under EU Medical Device Regulation Class I and are registered in the EUDAMED database. The manufacturer is based in Poland.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Paweł Pinkowski PPHU 'Alga' manufacture?

Paweł Pinkowski PPHU 'Alga' specializes in producing medical-grade wipes, specifically designed for single-use hygiene applications. These include standard wipes and those impregnated with additional substances (referred to as 'podfoliowane'). The devices are tailored for clinical and healthcare settings to maintain hygiene standards.

Where is Paweł Pinkowski PPHU 'Alga' based?

The company is based in Poland, operating as a manufacturer of medical devices within the country’s regulatory framework.

Which regulatory registries list devices manufactured by Paweł Pinkowski PPHU 'Alga'?

The company’s medical devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This ensures transparency and traceability of their products under EU medical device regulations.

How are the medical devices produced by Paweł Pinkowski PPHU 'Alga' classified under EU regulations?

The medical wipes produced by Paweł Pinkowski PPHU 'Alga' are classified as Class I devices under the EU Medical Device Regulation. This classification applies to low-risk devices that pose minimal risk to patients and users, such as single-use hygiene wipes, which do not require invasive procedures or prolonged contact with the body.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Poland(from EUDAMED actor address)
Address
18, Leśna, Wierzbno, Poland
PRRC contact
Weronika Duczmal
EUDAMED SRN
PL-MF-000046938