expert clinical advice

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FDA (USA), CE (European Union),
ISO 13485:2003,
CMDCAS, Health Canada,
EN 60601-3, India
FDA Indications

Class II medical device for home and clinic use to provoke penile erection in men with erectile dysfunction, and to provoke ejaculation in men with spinal cord injury.
CE Indications

Penile vibratory stimulation device for the treatment of erectile and ejaculatory disorders.