Objectives

The primary objective of this tender is to procure cuffed reinforced endotracheal tubes suitable for pediatric use, specifically designed for intubation procedures in children. The tubes must meet specified technical standards, ensure patient safety, and facilitate effective airway management in clinical settings.

Scope

The scope of the tender includes the supply of pediatric cuffed reinforced endotracheal tubes with specific dimensions and features, to be delivered to Grey’s Hospital in KwaZulu-Natal. The procurement covers different sizes (4mm and 4.5mm ID), with associated specifications such as length, OD, and features like radio-opaque lines and cuff mechanisms. The contract period is not specified, but the quotation validity is 90 days, and the supply is intended for use in hospital anesthesia and airway management.

Technical Requirements

• Product Description: Cuffed reinforced oral/nasal endotracheal tubes for pediatric patients.
• Sizes:
  • Size 4mm ID, OD 6mm, Length approximately 195mm
  • Size 4.5mm ID, OD 6.5mm, Length approximately 198mm
• Material & Sterility: Latex-free, sterile, individually packed in peel pouches, for single use, compliant with ISO 5361:2016 or equivalent.
• Design Features:
  • Spiral-wound reinforcing wire for flexibility and kink resistance
  • Radio-opaque line for visibility under imaging
  • Clear, durable markings indicating depth, size, length, ID, OD, and trade name
  • Precision or circumferential bands to aid with proper placement
  • Secure proximal end with 15mm OD circuit connector made from medical-grade plastic
  • Distal end with atraumatic beveled tip and Murphy eye
• Cuff Specifications:
  • High-volume-low-pressure barrel-shaped cuff with pilot cuff and one-way valve
  • Accurate inflation/deflation, resistant to Nitrous Oxide effects
  • Thickness approximately 50 microns
• Dimensions: Length varies (approximately 184mm to 198mm), with specific sizes for each tube.
• Additional Features: Markings must be clear, rub-proof, and aid in accurate placement; tubes must be kink resistant and atraumatic.
• Compliance: Must meet ISO 5361:2016 or equivalent standards; latex-free and sterile.