Center for medical device evaluation (CMDE) revised “Guidance for Registration of Intense Pulsed Light Equipment” and “Guidance for Registration of Ophthalmic Optical Instrument”.
For the details of the guidance, please consult the attachments.
Attachment:
Guidance for Registration of Intense Pulsed Light Equipment
Guidance for Registration of Ophthalmic Optical Instrument
Reference:
● NMPA Announcement on Issuing Guidance for Registration of Intense Pulsed Light Equipment (No. 12 of 2023)