RIMMEDTECH® BONE DUST TRAP
RIMMEDTECH® BONE DUST TRAP - AUTOLOGOUS BONE GRAFT COLLECTION DEVICE FOR SPINE SURGERY. THE NEXT-GENERATION INTRAOPERATIVE GRAFT RECOVERY SYSTEM IS DESIGNED TO HELP PRESERVE AUTOLOGOUS BONE MATERIAL WHILE FITTING SEAMLESSLY INTO THE STANDARD SURGICAL WORKFLOW
STEP 1 — Connect to Suction Line
Secure the device within the drape pouch using integrated fixation clip. The device is designed to support continuous intraoperative collection of autologous bone material while maintaining the existing surgical workflow.
STEP 2 — Secure & Collect
THREE EASY STEPS
STEP 3— Open & Use Collected Graft
Attach the surgical suction tubing to the outlet port designated "OUT." Attach the inlet tubing to the port designated "IN."
Disconnect, remove the lid, and access the collected autologous graft material for use according to the surgical plan.
Numerous studies consistently support the use of autologous bone graft, widely regarded as the "gold standard" in grafting procedures. Contact us for detailed scientific literature review.
TECHNICAL SPECIFICATIONS
Product: Rimmedtech® Bone Dust Trap
Product Category: Intraoperative autologous bone graft recovery system. Autologous bone graft collection device for orthopedic and spine surgery
Intended Use: Collection of locally generated autologous bone particulate during orthopedic and spine surgical procedures through the surgical suction pathway*
Applications: Spine surgery, orthopedic surgery, neurosurgery*
Container Capacity: 53 cc internal volume
Dimensions / in : 2.07 x 2.02 x 5.15
Filtration System: Patented dual-stage filtration
Connection: Compatible with standard surgical suction set up and tubing
Sterility: Sterile, irradiation
Single Use: Yes (per patient)
Latex: Not made with natural rubber latex
Materials: Medical-grade polymer construction
Packaging: Individually sterile packaged, double pouch
Manufacturer: RIM Medical Technologies Incorporated
Quality System: FDA QMSR Compliance, ISO 13485 certified manufacturing, process validation, biocompatibility and performance testing
Regulatory Status: FDA listed Class II, 510(k)-exempt device
Engineered to capture a range of bone fragment sizes, with design features intended to reduce clogging and support consistent collection of autologous bone material
ADVANCED DUAL-STAGE FILTRATION
Equipped with a rigid fixation clip and reinforced inlet and outlet ports, the device features a robust construction designed to support durability and reliable performance
ROBUST CONSTRUCTION
Intuitive design that keeps the operating field uncluttered and allows easy emptying and reuse within a single procedure on the same patient
SURGEON-CENTRIC ENGINEERING
53cc-volume container provides substantial capacity for intraoperative bone graft collection, accommodating a meaningful volume of autologous material and supporting consistent collection throughout the case without the need of interruptions
SUBSTANTIAL CAPACITY
Designed for convenient placement, the device fits securely into the draping pouch pocket for easy intraoperative access
CONVENIENT PLACEMENT
Manufactured with USP Class VI-tested materials in ISO 13485:2016-certified facilities, the Bone Dust Trap is tested for biocompatibility and performance