The Definitive Soft Tissue Protection Instrument for Exposing Entire Body Compartments
The KOCHER Retractor with 8 blunt prongs, 22.0 cm is a Class I medical device according to ISO 13485:2016. This extraordinary specialized instrument represents the pinnacle of atraumatic retraction technology. Eight fully blunt, broad-surface prongs are engineered to enable the exposure of large body cavities while simultaneously reducing any risk of injury to surrounding soft tissue, organs, and vascular structures to an absolute minimum.
Product Highlights:
✔ Certified according to ISO 13485:2016
✔ CE marking Class I (Regulation (EU) 2017/745)
✔ KOCHER premium design with superstable, ergonomic hammer handle
✔ 8 blunt prongs for maximum area coverage and minimal tissue pressure
✔ High-strength, biocompatible premium stainless steel 1.4435/316LVM (vacuum melted)
✔ Biocompatibility tested according to ISO 10993
✔ Fully blunt prongs with patented, tissue-adaptive contour
✔ Total length 22.0 cm for the deepest and most extensive surgical sites
✔ Autoclavable and reusable under strictest protocols
Advantages of the KOCHER Retractor (8 blunt prongs):
• Biomechanical Perfection: Eight broadly arranged prongs simulate an almost flat support, lowering specific tissue pressure below the critical ischemia threshold – ideal for prolonged procedures.
• Ultimate Protection for Parenchyma: Designed for direct contact with the most sensitive organs (liver, spleen, kidney, lung) in tumor and transplant surgery.
• Revolutionary Exposure Technique: Enables securing and retracting entire intestinal convolutes, the greater omentum, or mobilized organ blocks in a single, controlled motion.
• Prevention of Secondary Complications: Significantly reduces the risk of postoperative adhesions, seroma formation, and tissue necrosis through minimal-pressure application.
• Engineering Marvel: Each of the eight prongs is computer-designed and aligned for optimal force distribution.
Technical Specifications:
• Model: KOCHER Retractor with Hammer Handle (Master-Protection Model)
• Type: 8 blunt prongs
• Total Length: 22.0 cm
• Handle: Superstable, textured Hammer Handle for precise bimanual control
• Prong Shape: Eight wide, parallel, fully blunt prongs with concave adaptation geometry
• Material: High-strength surgical premium stainless steel 1.4435 / 316LVM
• Surface: High-gloss polished, electropolished, with diamond-coated passivation
• Processing: Autoclavable up to 135°C. Mandatory: Dedicated manual pre-cleaning protocol + validated cleaning-disinfection process in a special single tray.
• Special Feature: The most advanced instrument for maximum soft tissue protection in high-risk surgery
• Risk Class: I according to Regulation (EU) 2017/745 (MDR)
Fields of Application (Extremely Specialized):
• Radical oncological visceral surgery with multivisceral resection
• Highly complex transplant surgery (multi-organ procurement, living donor liver transplantation)
• Extensive Cytoreductive Surgery (CRS) with Hyperthermic Intraperitoneal Chemotherapy (HIPEC)
• Revision procedures following multiple previous surgeries with extremely vulnerable conditions
• Specialized thoraco-abdominal trauma surgery
CRITICAL NOTES AND SAFETY PROTOCOLS:
• FOR USE BY HIGHLY QUALIFIED SURGEONS IN CERTIFIED MAXIMUM CARE CENTERS ONLY.
• NOT A GENERAL SURGICAL INSTRUMENT. Use requires strictly documented indication and risk-adapted assessment.
• PRE-OPERATIVE INSPECTION MANDATORY: Before each use, all eight prongs must be inspected under magnifying loupes for perfect surface integrity, exact alignment, and structural homogeneity.
• APPLICATION TECHNIQUE: Requires special training. Only vertical, flat traction is permitted. Absolute contraindication for prying movements.
• REPROCESSING PROTOCOL: Highest hygiene standards. The instrument requires a dedicated reprocessing protocol from the OR table to sterilization. Regular inspection by manufacturer service.
• DISCARD POLICY: In case of any deviation from target geometry, micro-scratches, polish alterations, or even suspicion of material fatigue, the instrument must be immediately and permanently withdrawn from use and returned to the manufacturer for analysis. Do not reuse under any circumstances.
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