Foshan ZIANN Medical Apparatus Co., Ltd.

Foshan ZIANN Medical Apparatus Co., Ltd. produces a range of Class IIa medical devices. Based on the naming conventions and typical industry patterns, their devices appear to include electrosurgical or radiofrequency instruments, such as the ZA-208 series (e.g., ZA-208Q3, ZA-208B) and the standalone ZIANN model. These devices are likely designed for controlled surgical or procedural applications where precise energy delivery is required.

The company is headquartered in China, specifically in Foshan. This location is relevant for understanding its regulatory context, manufacturing operations, and compliance with local and international medical device standards.

Yes, Foshan ZIANN Medical Apparatus Co., Ltd.’s devices are registered in the euamed database. This registry is part of the European Union’s medical device transparency system, where manufacturers list their Class IIa devices to ensure traceability and compliance with EU regulations. Listing in euamed does not imply approval but confirms regulatory engagement.

The company’s devices fall under Class IIa classification in the EU regulatory framework. This classification is assigned based on risk assessment criteria—Class IIa devices pose a moderate risk and require compliance with specific design controls, clinical evaluations, and conformity assessment procedures to ensure safety and performance before market placement.