Class 6841 Medical Devices

A range of Class I medical devices including basic medical instruments and equipment manufactured under regulated quality systems. Products comply with medical device classification and regulatory requirements.

Low-risk classified medical devices meeting regulatory standards for household medical applications. These products include basic medical instruments and equipment for consumer health monitoring.

Design and manufacturing of Class I medical device components and assemblies meeting regulatory requirements and clinical standards.

Range of Class II medical devices developed and manufactured according to regulatory standards. These moderately-risk devices undergo predefined quality controls and clinical evaluation procedures.

General medical instruments meeting international quality and safety standards. Manufactured with advanced machining processes and certified ISO 13485:2016 and CE Class I for sterile and non-sterile applications.

Distribution and retail supply of Class I medical devices, which are the lowest-risk category of medical devices subject to general controls. The company serves as a wholesale and retail supplier of these general medical devices.

Portfolio of Class I medical devices developed and manufactured according to medical device quality management standards. Includes various antimicrobial medical applications.

Complete configuration solutions for Class I medical devices and equipment systems designed according to specific clinical and institutional requirements.

Specialized medical devices designed for gynecological applications and procedures. These devices support diagnosis and treatment in obstetric and gynecological clinical practice.

Control units and special fittings developed for sensitive medical applications. Products are manufactured to meet the highest quality requirements and international standards for medical device applications.

Complete or partial assemblies of Class I medical devices manufactured according to regulatory standards. Produced with comprehensive quality documentation and traceability.

ISO 13485-certified series production of medical devices with cleanroom facilities, internalized manufacturing processes, and sterilization-ready output.