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Manufacturing Facility
Our facility specializes in Disposable Surgical systems for effective debridement following orthopedic procedures of trauma and joint arthroplasty. Established in 2004, all products are certified by CE & ISO13485.
Our systems combine convenience and power for the removal of contaminated water, necrotic tissue, bone debris, and wound pollutants while providing controlled pressure for efficient cleansing on flat wound surfaces or intra-medullary sites. Products are continuously improved via clinical research and feedback, with minimized noise and weight (currently only 772g) for better surgical handling.
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Frequently Asked Questions
What material is the suture anchor made of?
The suture anchor is made of high-quality Titanium, ensuring durability and biocompatibility for orthopedic procedures.
What certifications does this product hold?
The product is fully certified with CE and ISO13485 standards, meeting international medical device requirements.
Is the suture anchor reusable or disposable?
It is a disposable medical device, sterilized using EO (Ethylene Oxide) for maximum safety and hygiene.
What are the available sizes for the suture anchors?
We offer a wide range of specifications including 1.8mm, 2.8mm, 3.5mm, 4.0mm, 4.5mm, 5.0mm, 5.5mm, and 6.5mm.
What is the shelf life of the product?
The suture anchor has a validity period of 3 years from the date of manufacture.
What is the primary function of this orthopedic implant?
The primary function is to securely connect soft tissue and bone during orthopedic surgeries.
Sete Orthopedic Implants
