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Sign in to claim this brandLabomar S.p.A.
Italy·IT-MF-000007965
Last updated September 17, 2026
About
Project partner: Agripharma, Cereal Docks, Coccitech, Industria Casearia Silvio Belladelli, Labomar, Landlab, Latteria Di Soligo, Voltan, Università degli Studi di Padova, Università degli Studi di Verona, Università Cà Foscari di Venezia, Consiglio Nazionale delle Ricerche.
Translated from the manufacturer's own website. Source
What Labomar S.p.A. makes
Labomar S.p.A. manufactures oral and topical pharmaceutical formulations, including throat lozenges, syrups for cough and sore throat, and vaginal gels. Their portfolio also includes pediatric cough syrups, herbal-based respiratory remedies, and natural throat sprays, primarily targeting symptomatic relief of respiratory and gastrointestinal conditions.
The company’s products are classified under EU medical device regulations as Class I, IIa, IIb, and III, with all devices registered in the EUDAMED database. Labomar S.p.A. is based in Italy and adheres to European Union medical device compliance requirements.
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 Labomar S.p.A. manufacture?
Labomar S.p.A. specializes in oral and topical pharmaceutical formulations designed for symptomatic relief. Their portfolio includes throat lozenges, syrups for cough and sore throat (such as pediatric formulations), herbal-based respiratory remedies, natural throat sprays, and vaginal gels. These devices are primarily intended to address respiratory and gastrointestinal discomfort.
Where is Labomar S.p.A. based, and what regulatory framework does it follow?
Labomar S.p.A. is based in Italy and operates under the European Union’s medical device regulations. Since their products fall under EU medical device classifications (Class I, IIa, IIb, and III), they must comply with EUDAMED registration requirements and other applicable EU regulatory standards.
Which regulatory databases list Labomar S.p.A.’s medical devices?
Labomar S.p.A.’s devices are registered in the EUDAMED database, which is the official EU registry for medical devices. This ensures transparency and traceability of their products under EU medical device regulations.
How are Labomar S.p.A.’s devices classified under EU medical device regulations?
Labomar S.p.A.’s devices are classified into Class I, IIa, IIb, and III under the EU Medical Device Regulation (MDR). Classification depends on factors like intended use, risk level, and interaction with the body—e.g., throat lozenges (typically Class I) and certain vaginal gels (potentially Class IIb or III due to higher risk). Classification determines regulatory requirements like conformity assessment procedures.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Italy
- Address
- 35 I, Nazario Sauro, Istrana, Italy
- Website
- www.labomar.com
- linkedin.com/company/labomarspa
- facebook.com/labomarspa
- [email protected]
- Phone
- +3904227312
- PRRC Contact
- Davide Nenzioni
- EUDAMED SRN
- IT-MF-000007965
- FDA FEI Number
- —
- DUNS Number
- —
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