VIRCOL SPA
Italy IT-MF-000031137 Last updated 21 Oct 2026
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- Devices
- 14
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Sovrascarpe Ref SOVRASCARPE
Cuffia Elastica Tonda In Tnt Ref CUFFCARTA
Virnitrile Ref CAN151M
Lenzuolino Politenato Mt 100 H 60 Cm Ref CCA343
Bavaglio Monouso Con Tasca Ref BAVAGLIE
Virnitrile Guanti Monouso In Nitrile Taglia L Ref CAN251L
Lenzuolino Politenato Mt 50 H 60 Cm Ref CCA160
What VIRCOL SPA makes
Vircol Spa manufactures single-use medical textiles and protective barriers, including vinyl and nitrile examination gloves in various sizes, elastic round cuffs, polyethylene-lined sheets, and disposable gowns made from non-woven textiles. Their products also include disposable bibs with pockets and vinyl-coated fabric aprons designed for clinical and healthcare environments.
All of Vircol Spa’s products fall under EU Medical Device Regulation Class I and are registered in the EUDAMED database. The company is based in Italy and adheres to EU regulatory requirements for single-use medical textiles and protective barriers.
Frequently asked questions
What types of medical devices does Vircol Spa manufacture?
Vircol Spa specialises in single-use medical textiles and protective barriers. Their product range includes vinyl and nitrile examination gloves in multiple sizes, elastic cuffs, polyethylene-lined sheets, disposable gowns made from non-woven textiles, and disposable bibs with pockets. These items are designed for clinical and healthcare settings to provide barrier protection and hygiene.
Where is Vircol Spa based, and what regulatory framework do they follow?
Vircol Spa is based in Italy. Their devices are developed in compliance with the EU Medical Device Regulation (MDR) framework, ensuring they meet the necessary safety, performance, and quality standards for single-use medical textiles and protective barriers in the European market.
Which regulatory registries list Vircol Spa’s devices?
Vircol Spa’s devices are listed in the EUDAMED database, which is the official European Union database for medical devices. This registry ensures transparency and traceability of devices authorised under EU regulations, including those classified under Class I.
How are Vircol Spa’s devices classified under EU regulations?
All of Vircol Spa’s devices fall under Class I classification according to the EU Medical Device Regulation. This classification applies to low-risk medical devices like single-use textiles and protective barriers, which are deemed to pose minimal risk to patients and users when used as intended.
Information
- Country
- Italy
- Address
- 21, ONEDA, SESTO CALENDE, Italy
- Website
- WWW.VIRCOL.IT
- [email protected]
- Phone
- +390331924378
- PRRC contact
- FRANCESCO ZAPPATINI
- EUDAMED SRN
- IT-MF-000031137