Indication: Specifically designed for low limbs fracture treatment and lengthening procedures.
Technical Specs: Optimized for fractures relevant to the articular surface. Utilizes a 4.8mm drill bit and is compatible with olive-head Kirschner wire when necessary.
Screw Compatibility: Supports 6.0/5.0 screws in both Stainless Steel (SS) and Titanium Alloy (TA).
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Manufacturing Excellence
Operating strictly according to the ISO13485 quality system, we adhere to the highest specifications of medical device manufacturing and the CE MDD 93/42/EEC directive.
Our facilities feature advanced processing equipment, including German and American-imported machining centers and Japanese-imported automatic lathes. Our comprehensive testing center includes a biomechanical laboratory and a physical-chemical testing center to ensure:
Strict raw material procurement control
Rigorous product quality monitoring
Advanced new product performance analysis
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Global Congress & OEM
Our orthopedic solutions are exported globally to countries including France, Turkey, Indonesia, Mexico, Russia, and Thailand. Feedback confirms our products meet or exceed local international standards. We also serve as a major OEM supplier for global industry leaders.
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Frequently Asked Questions
Q1: What materials are the Multi-ring Combined Fixators made of?A1: Our fixators are available in high-grade Pure Titanium, Titanium Alloy, and Stainless Steel to suit different clinical requirements.
Q2: Is the device delivered sterile?A2: The product is typically provided in a non-sterile package using paper-plastic roll bags. It must be sterilized before use according to hospital protocols.
Q3: What are the primary indications for this fixator?A3: It is primarily indicated for lower limb fractures, especially those involving the articular surface, and for bone lengthening procedures.
Q4: Does the system support different screw sizes?A4: Yes, the system is compatible with both 5.0mm and 6.0mm screws in either Stainless Steel or Titanium Alloy.
Q5: Are your manufacturing processes internationally certified?A5: Yes, all manufacturing follows ISO13485 standards and complies with the CE MDD 93/42/EEC directive for medical devices.
Q6: Can this device be used for pediatric patients?A6: This specific model (17.201.23) is categorized for Adult use. Please consult our catalog for pediatric-specific solutions.
Weed Orthopedic Implants
