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Fater S.p.A.

Italy IT-MF-000014121 Last updated 17 Sep 2026

Devices
168
Registries
EUDAMED
FDA recalls
0

Catalogue168

Page 3 of 4

Showing 101-150 of 168

What Fater S.p.A. makes

Fater S.p.A. manufactures a range of disposable incontinence products, including waistbanded pads, rectangular absorbent pads with barrier protection, and various sizes of adult diapers and protective underwear. Their portfolio also includes specialized liners, such as the LINIDOR line, designed for different levels of absorption and wearer needs, as well as nighttime and slip-resistant protective solutions for women.

The company’s products are classified under Class I medical devices and are registered in the EUDAMED database. Fater S.p.A. is based in Italy and adheres to European regulatory requirements for these devices.

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 Fater S.p.A. manufacture?

Fater S.p.A. specializes in disposable incontinence products. Their portfolio includes waistbanded pads like the Pannolone a Cintura, rectangular absorbent pads with barrier protection such as the Classic Rettangolare, and specialized liners like the LINIDOR line, which cater to varying absorption needs. They also produce adult diapers, protective underwear, and gender-specific solutions like the LADY range for women, including nighttime and slip-resistant options.

Where is Fater S.p.A. based, and how does that affect its regulatory compliance?

Fater S.p.A. is based in Italy, which means its devices must comply with European Union medical device regulations. Since their products fall under Class I classification, they are subject to EU requirements for conformity assessment and must be listed in the EUDAMED database to demonstrate regulatory transparency and traceability.

Which regulatory registries list Fater S.p.A.’s devices, and why is this important?

Fater S.p.A.’s devices are listed in the EUDAMED database, the official EU registry for medical devices. This registry ensures visibility of authorized products, helps healthcare professionals verify compliance, and supports transparency in the supply chain. Listing in EUDAMED is mandatory for Class I devices under EU regulations.

How are Fater S.p.A.’s incontinence products classified under EU regulations?

Fater S.p.A.’s incontinence products are classified as Class I medical devices. This classification applies because they are low-risk, non-invasive disposable items designed for temporary use in managing incontinence. Class I devices require basic regulatory compliance, including conformity assessment and registration in EUDAMED, but do not require third-party certification.

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

Information

Country
Italy(from SRN)
Address
122, MARE ADRIATICO , SPOLTORE, Italy
Website
pec-fater.it
PRRC contact
GIANBATTISTA AICARDI
EUDAMED SRN
IT-MF-000014121