Laser

1. Model:FDA,Medical CE,TGA,TUV approved 755+808+1064 three wavelengths diode laser machine.

MDSAP is a single audit program that consists of one single regulatory audit of medical device quality management systems to meet relevant requirements of multiple regulatory authorities. Established by the International Medical Device Regulators Forum (IMDRF), the MDSAP supports a global auditing and monitoring approach for medical device manufacturing to assess the compliance of products used in the medical field.

2. Skin type:1-6

Razorlase (patent name)hair removal machine is medical grade, suitable for World Health Organization skin classification standard 1-6, which is from white skin to black skin.

One of our biggest advantage is we do have medical degree suggestion parameters system in our machine, after you choose the skin type and treatment area, the machine will give you a safe suggestion parameters , you can start the treatment by this parameters.It is easy for beginner operator.

3. Self-testing system

MDSAP is a single audit program that consists of one single regulatory audit of medical device quality management systems to meet relevant requirements of multiple regulatory authorities. Established by the International Medical Device Regulators Forum (IMDRF), the MDSAP supports a global auditing and monitoring approach for medical device manufacturing to assess the compliance of products used in the medical field.

4. After-sales process

MDSAP is a single audit program that consists of one single regulatory audit of medical device quality management systems to meet relevant requirements of multiple regulatory authorities. Established by the International Medical Device Regulators Forum (IMDRF), the MDSAP supports a global auditing and monitoring approach for medical device manufacturing to assess the compliance of products used in the medical field.

5. Imported parts:

MDSAP is a single audit program that consists of one single regulatory audit of medical device quality management systems to meet relevant requirements of multiple regulatory authorities. Established by the International Medical Device Regulators Forum (IMDRF), the MDSAP supports a global auditing and monitoring approach for medical device manufacturing to assess the compliance of products used in the medical field.