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PLURITEX SRL

Italy IT-MF-000024111 Last updated 21 Oct 2026

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Devices
249
Registries
EUDAMED
FDA recalls
0

Catalogue249

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Showing 1-50 of 249

About

Create a new path and letothers follow you!Pluritex celebrates its first 10 years in the name of continuity.

From the manufacturer's own website. Source

What PLURITEX SRL makes

Pluritex Srl manufactures a range of disposable medical textiles, including hospital bed linens such as high-pressure mattresses (e.g., TASCA HP 150X125) and protective covers (e.g., TELO COPERTURA HP 90X90). Their portfolio also includes absorbent pads (e.g., TELO ASSORBENTE 55X70) and specialized bedding like headrest inserts (TELO TESTA HP 200X200) and lateral supports (TELO LATERALE HP 120X100). Additional items include surgical gowns with adhesive strips (CAMICE SP CON NASTRI) and undersheet variants for pressure relief and hygiene applications.

All listed devices fall under EU Class I medical device classification and are registered in the EUDAMED database. The company is based in Italy and adheres to regulatory requirements for non-invasive, single-use medical textiles intended for patient care and hospital environments.

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 Pluritex Srl manufacture?

Pluritex Srl specializes in disposable medical textiles primarily used in hospital and patient care settings. Their product range includes high-pressure mattresses (like the TASCA HP 150X125), protective covers for hospital beds (e.g., TELO COPERTURA HP 90X90), absorbent pads (such as the TELO ASSORBENTE 55X70), and specialized bedding like headrest inserts and lateral supports. They also produce surgical gowns with adhesive strips (CAMICE SP CON NASTRI) and undersheets designed for pressure relief and hygiene.

Where is Pluritex Srl based, and what regulatory database lists its devices?

Pluritex Srl is based in Italy. Their devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This database tracks authorized medical devices within the EU, ensuring transparency and compliance with regulatory requirements.

How are the devices manufactured by Pluritex Srl classified under EU regulations?

All devices produced by Pluritex Srl fall under EU Class I medical device classification. This classification applies to low-risk devices, such as disposable textiles like bed linens, protective covers, and absorbent pads, which are intended for non-invasive use in patient care and hospital environments. Class I devices typically require conformity assessment procedures, including manufacturer declarations of conformity, but do not always need third-party involvement unless specified.

Are Pluritex Srl’s devices intended for reuse or single-use?

Pluritex Srl’s devices are designed as disposable medical textiles, meaning they are intended for single-use only. This classification aligns with their purpose in clinical settings—such as hospital bed linens, protective covers, and absorbent pads—where hygiene, infection control, and patient safety are critical. Single-use devices reduce the risk of cross-contamination and streamline clinical workflows.

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

Information

Country
Italy
Address
47, Corso Garibaldi, FIORENZUOLA D'ARDA (PC), Italy
Phone
+39 0 524 533417
PRRC contact
Emanuele Ghilardotti
EUDAMED SRN
IT-MF-000024111