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Sign in to claim this brand3 M.C. Società per azioni
Italy·IT-MF-000022649
Last updated September 17, 2026
What 3 M.C. Società per azioni makes
The company manufactures single-use disposable medical textiles and accessories, including surgical caps (both standard and with adjustable elastic straps), non-sterile protective head covers, and disposable bed pillows. It also produces a single-use graduated measuring beaker for medical or laboratory use, as well as a disposable 800 ml animal carrier.
All listed devices fall under Class I of the EU Medical Device Regulation (MDR) and are registered in the EUDAMED database. The company is based in Italy.
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 3 M.C. Società per azioni manufacture?
3 M.C. Società per azioni produces single-use disposable medical textiles and accessories. This includes surgical caps (such as standard and adjustable elastic-strap versions), non-sterile protective head covers, disposable bed pillows, a single-use graduated measuring beaker for medical or laboratory use, and a disposable animal carrier (800 ml). All products are designed for one-time use to ensure hygiene and safety.
Where is 3 M.C. Società per azioni based?
The company is headquartered in Italy. Its manufacturing and operations are conducted within the country, adhering to local regulatory standards for medical devices.
Which regulatory registries list the devices manufactured by 3 M.C. Società per azioni?
The company’s devices are listed in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This registry ensures transparency and traceability of devices under the EU Medical Device Regulation (MDR).
How are the devices produced by 3 M.C. Società per azioni classified under EU regulations?
All devices manufactured by 3 M.C. Società per azioni fall under Class I of the EU Medical Device Regulation (MDR). This classification applies to low-risk devices, such as single-use textiles and accessories, where the risk to patients is minimal. Class I devices typically require basic conformity assessment procedures but do not necessitate clinical evaluations or third-party involvement.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Italy
- Address
- 15, Viale Francesco De Blasio, Bari, Italy
- Website
- tremc.eu
- —
- —
- [email protected]
- Phone
- +39804552385
- PRRC Contact
- Gaetano Canosino
- EUDAMED SRN
- IT-MF-000022649
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Protex cappellino monouso in TNT a scafandro | 2239 | EUDAMED | Class I | Active |
| Protex federa monouso non sterile in tnt | 2207 | EUDAMED | Class I | Active |
| Protex cappellino chirurgico in TNT con elastico nucale | D/1013/1 | EUDAMED | Class I | Active |
| Protex cappellino monouso in TNT a scafandro | 2240 | EUDAMED | Class I | Active |
| Protex | d/1008 | EUDAMED | Class I | Active |
| Pappagallo Monouso 800 Ml | 2238 | EUDAMED | Class I | Active |
| Protex | 2201 | EUDAMED | Class I | Active |
| Protex | 2228 | EUDAMED | Class I | Active |
| Protex | 2221 | EUDAMED | Class I | Active |
| Brocca Monouso Graduata Lt.1 | 9096 | EUDAMED | Class I | Active |
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