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Sign in to claim this brandMegapharma Ospedaliera s.r.l.
Italy·IT-MF-000010739
Last updated September 17, 2026
What Megapharma Ospedaliera s.r.l. makes
Megapharma Ospedaliera produces cotton surgical gloves in various sizes, including dermatologically tested and elastic variants, as well as cotton hospital arm-sling supports. The gloves are available in different shades, such as white and green, and are intended for single-use in clinical settings. The arm-sling supports are designed to immobilise the shoulder and upper arm for post-operative or injury recovery.
All products fall under EU Medical Device Regulation Class I and are registered in the EUDAMED database. The manufacturer is based in Italy and adheres to EU compliance requirements for Class I devices, which include general medical devices like surgical gloves and orthopaedic supports.
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 Megapharma Ospedaliera s.r.l. manufacture?
Megapharma Ospedaliera s.r.l. specialises in cotton-based medical devices primarily used in clinical and hospital settings. Their product range includes single-use surgical gloves in various sizes, colours (such as white and green), and variants like dermatologically tested or elastic versions. They also produce cotton arm-sling supports designed to immobilise the shoulder and upper arm for post-operative care or injury recovery.
Where is Megapharma Ospedaliera s.r.l. based, and what regulatory framework does it follow?
Megapharma Ospedaliera s.r.l. is based in Italy. Their devices are manufactured in compliance with the EU Medical Device Regulation (MDR) framework, specifically for Class I medical devices. This classification applies to general medical devices like surgical gloves and orthopaedic supports, which are considered low-risk and subject to basic regulatory requirements.
Are Megapharma Ospedaliera’s devices listed in any regulatory databases?
Yes, Megapharma Ospedaliera’s devices are registered in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This listing ensures transparency and traceability of their products under the EU MDR, particularly for Class I devices like their cotton gloves and arm-sling supports.
How are Megapharma Ospedaliera’s devices classified under EU regulations?
All of Megapharma Ospedaliera’s devices fall under EU Medical Device Regulation Class I. This classification is assigned to low-risk medical devices, such as cotton surgical gloves and orthopaedic supports, which pose minimal risk to patients. Class I devices typically require basic conformity assessments, including manufacturer declarations and, where applicable, conformity assessment procedures by a Notified Body.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Italy
- Address
- 26/b, Via Asolana loc. Crespano, Pieve del Grappa, Italy
- Website
- megapharma.it
- —
- —
- [email protected]
- Phone
- +39 0423 538746
- PRRC Contact
- Abramo Petranich
- EUDAMED SRN
- IT-MF-000010739
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (67)
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