Product Overview

The UNITRAC® Holding Device, coupling element is a reusable surgical system component configured as coupling element. It is intended for integration into the applicable surgical holding or retraction-system configuration. The product is specified for Spine Surgery, Neurosurgery, Maxillo-Facial Surgery, Vascular Surgery, Urology, Cardiac / Thoracic Surgery, Hand / Foot Surgery, Plastic Surgery, Pediatric Surgery, Orthopaedics / Traumatology, Ear-Nose-Throat Surgery, General / Visceral Surgery, Gynaecology and is supplied non-sterile for validated processing before clinical use.

Design and Configuration

The specified type is coupling element, defining the primary configuration of the product. Internal compatibility codes supplied in the source data are excluded from customer-facing content. No unsupported dimensions, materials, or mechanical specifications are stated.

Surgical Applications

The product is specified for Spine Surgery, Neurosurgery, Maxillo-Facial Surgery, Vascular Surgery, Urology, Cardiac / Thoracic Surgery, Hand / Foot Surgery, Plastic Surgery, Pediatric Surgery, Orthopaedics / Traumatology, Ear-Nose-Throat Surgery, General / Visceral Surgery, Gynaecology. Its use should follow the applicable surgical-system configuration, surgical technique, and healthcare-facility protocols.

Handling and Care

The component is identified as reusable and non-sterile. Before clinical use, inspect it for cleanliness, integrity, and suitability. Following use, cleaning, inspection, maintenance, packaging, and sterilization should be performed according to validated procedures for reusable surgical instruments and system components.

Technical Specifications

The product is configured as coupling element for the specified surgical applications.

It is supplied as a reusable, non-sterile component for appropriate validated processing.