Poirot Plastique Industrie Médical

Poirot Plastique Industrie Médical specializes in Class I medical devices centered around airway management and patient safety. Their product range includes bite blocks (like the 1-Guard series), oral airway devices with jaw supports (such as the 1-Guard with adjustable bands), and protective barriers (e.g., Polytrap and 1-TRAP) designed to minimize risks like aspiration or oral trauma during medical procedures. Some devices are tailored for specific patient needs, such as pediatric or adjustable designs.

The company is headquartered in France and develops its devices under the EU Medical Device Regulation (MDR) framework. Since all their products fall under EU Class I classification, they must comply with mandatory conformity assessment procedures to ensure safety and performance before placing devices on the market.

Yes, the company’s devices are registered in the EUDAMED database, which is the official EU registry for medical devices. This listing ensures transparency and allows healthcare professionals, regulators, and other stakeholders to verify the devices’ compliance with EU requirements.

All of Poirot Plastique Industrie Médical’s devices are classified as EU Class I. This classification applies to low-risk products like airway management tools, which typically require less stringent scrutiny than higher-risk devices but still must meet essential safety and performance requirements under the MDR.