Scharf Surgical Instruments®

At Scharf Hair Transplant & Plastic Surgery Instruments, we have been committed to delivering top-quality products at reasonable prices since our foundation in 2011. Using the finest materials, we aim for maximum excellence in developing and producing hair transplant instruments.

Customer satisfaction has always been our priority, and our rapid growth—serving over 95 countries—reflects the success of our mission. We offer a wide range of high-quality products and continually refine our designs based on advancements in the field and feedback from our customers.

Our open communication with clients and collaboration with industry colleagues keep us at the forefront of innovation. We value new ideas and are dedicated to maintaining excellence through the expertise and ongoing training of our skilled staff. Our years of experience, research, and dedication are evident in the efficiency and quality of our instruments.

Our Logistics

Thanks to our efficient delivery system, we ensure fast and reliable order fulfillment. Most items in our extensive product range are readily stocked, allowing for quick delivery via the shortest possible routes while accommodating customer requests. We deliver within 24-72 hours: tax- and duty-free across Europe from our Germany office, to the Middle East from our UAE office, and to North America and Canada from our USA office.

We value close customer connections and actively participate in trade fairs, international hair transplant conferences, and workshops worldwide. Our engineers and doctors collaborate with surgeons at these events to continuously enhance our product quality.

FDA Approved

The United States Food and Drug Administration (FDA) is a federal agency under the Department of Health and Human Services. It ensures public health by regulating food safety, tobacco products, dietary supplements, medications, vaccines, biopharmaceuticals, blood transfusions, medical devices, cosmetics, and veterinary products.

ISO 13485:2004

ISO 13485:2004 defines requirements for a quality management system in medical device organizations, ensuring products and services consistently meet customer and regulatory standards. It applies to all stages of the life cycle, including design, production, distribution, and servicing, as well as related activities like technical support.

ISO 18001:2007

OHSAS 18001:2007 is a global standard for occupational health and safety management, helping organizations manage risks, reduce accidents, ensure legal compliance, and enhance performance.

ISO 14001:2004

ISO 14001:2004 outlines requirements for an environmental management system, enabling organizations to create policies and objectives that consider legal and significant environmental aspects they can control or influence.

ISO 9001:2008

Scharf FUE Instruments’ ISO 9001:2008-certified quality management system ensures consistent product quality, compliance with customer and regulatory requirements, and enhanced customer satisfaction through continual improvement

ISO 17664:2017

ISO 17664:2017 outlines requirements for information that medical device manufacturers must provide to ensure safe processing and maintain device performance during resterilization.

TSE_HYB

Scharf FUE Instruments is certified from Turkish Standards Institution (TSE).

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