LadySystem Pelvic Floor Therapy is a Class 1 medical device which satisfies the requirements of the European medical device Directive 93/42/EEC, and bears the CE Mark to indicate its compliance with the requirements of that directive.
The materials used in the manufacture of LadySystem Pelvic Floor Therapy comply with international standards of pharmacological safety, including United States Pharmacopoeia XXII Class VI, FDA, and ISO 10993 (biocompatibility).
LadySystem Pelvic Floor Therapy has been used and recommended by medical specialists since 1994. It is our policy continuously to develop the product in order to optimise its safety, quality, and effectiveness, and we maintain a close dialogue with medical professionals and users of the product in order to achieve that aim.
Ladysystem Pelvic Floor Therapy cones are of robust design and construction and have been extensively tested for safety in regular every day use.
