Welcome to the Citieffe website.
The information provided on this site is intended solely for the use of healthcare professionals.
By accessing or using this site, the user declares, under his own responsibility, to be in possession of one of the qualifications for the consultation and saving of documents.
A healthcare professional must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient.
Citieffe does not dispense medical advice and recommends that healthcare professionals be trained in the use of any particular product before using it in a procedure or surgery.
A healthcare professional must always refer to the package insert, product label and/or instructions for use, including the instructions for cleaning and sterilisation (if applicable), before using any Citieffe product.
The information presented is intended to demonstrate Citieffe product offerings.
Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets.
Please contact your Citieffe representative if you have questions about the availability of specific products in your area.
Quality management system
Citieffe Quality Management System complies with UNI EN ISO 9001: 2015 and UNI CEI EN ISO 13485: 2021, with 21 CFR 820, 21 CFR 803, 21 CFR 806, and with RDC 665/2022 for the design, production and sale of implantable medical devices and surgical instruments for orthopedics and traumatology.
The complete quality assurance system of Citieffe products complies with the applicable requirements of Regulation (EU) 2017/745.
The quality of the products and services provided by Citieffe represents a guarantee for patients and healthcare professionals; therefore constitutes a strategic objective which ensures the maintenance of excellent product standards.