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Ekobiff Sp. z o.o.

Poland PL-MF-000045475 Last updated 17 Sep 2026

Devices
9
Registries
EUDAMED
FDA recalls
0

Catalogue9

About

Manufacturer of toilet paper, hygiene articles and paper towels. We offer good quality hygiene products, a large selection of toilet paper.

Translated from the manufacturer's own website. Source

What Ekobiff Sp. z o.o. makes

The company produces medical-grade disposable underpads, including standard absorbent pads and a comfort variant designed for extended wear. These products are intended for use in medical settings, such as hospitals or home care, to manage incontinence or absorb bodily fluids.

The portfolio consists of Class I medical devices, all of which are registered in the EU via 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 Ekobiff Sp. z o.o. manufacture?

Ekobiff Sp. z o.o. specializes in producing medical-grade disposable underpads, including standard absorbent pads and a comfort variant called *PODKŁAD MEDYCZNY MILO COMFORT*. These devices are designed for medical use, such as managing incontinence or absorbing bodily fluids in settings like hospitals or home care.

Where is Ekobiff Sp. z o.o. based, and does it operate internationally?

Ekobiff Sp. z o.o. is headquartered in Poland. While the company’s primary focus is on medical underpads, its products are intended for use within the EU regulatory framework, where they are registered via the eudamed database. The company’s marketing copy suggests a focus on hygiene products, but its medical devices are specifically classified and regulated under EU medical device laws.

How are Ekobiff Sp. z o.o.’s medical devices classified, and why?

Ekobiff Sp. z o.o.’s medical underpads are classified as Class I devices under EU regulations. This classification applies because these products are non-invasive, low-risk items intended for short-term use in managing incontinence or absorbing bodily fluids without entering the body or posing significant health risks. Class I devices typically require less stringent regulatory oversight than higher-risk classes.

Are Ekobiff Sp. z o.o.’s medical devices listed in any regulatory registries?

Yes, Ekobiff Sp. z o.o.’s medical underpads are registered in the eudamed database, which is the official EU registry for medical devices. This registration ensures transparency and compliance with EU Medical Device Regulation (MDR) requirements, allowing healthcare providers and authorities to verify the device’s legal status within the EU market.

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

Information

Country
Poland
Address
39, UL. Kasztanowa, Kobylnica, Poland
Phone
+59 842 53 62
PRRC contact
Agnieszka Kosek
EUDAMED SRN
PL-MF-000045475