Product Description
XZ498-18-415 Screw size:18-415 Ejection dose:0.10ml/t Chongqing Xinjitai Pharmaceutical Sprayer&Pump Co.,Ltd 1.27years in manufacturing sprayers 2.30% Chinese market 3.50% of Chinese top-100 pharma 4. Purification workshop of 10, 000 level 5. Packaging for GMP (ISO 15378) 6. Over 100 million of annual production 7. Own mould making 8. Strong R&D for special request, 9.market management xjtsprayer@xinjitai-jp.com Mob:+86-013510688512 Whatsapp:86+13510688512 LINE:medicinalpackaging
AI Product Description
*The following content is generated by AI and is for reference only.
The XZ498-18-415 throat sprayer is a specialized medical device designed for the targeted delivery of liquid medications, anesthetics, or antiseptic solutions directly to the pharynx and larynx. Primarily utilized in clinical settings such as emergency rooms, operating theaters, and outpatient clinics, this instrument ensures precise administration of treatments for conditions like severe sore throats, vocal cord inflammation, or pre-procedural anesthesia. Its ergonomic design facilitates easy handling by healthcare professionals, allowing for accurate aiming even in difficult anatomical positions without causing unnecessary trauma to sensitive tissues. The device typically features a durable, corrosion-resistant nozzle that withstands repeated sterilization cycles, ensuring long-term hygiene and patient safety.
When using this equipment, strict adherence to safety protocols is essential to prevent complications. Operators must verify the compatibility of the medication with the sprayer mechanism before each use to avoid chemical reactions or clogging. It is crucial to maintain a sterile environment during operation; the nozzle should be disinfected thoroughly between patients using approved hospital-grade agents to cross-contamination risks. Users should also ensure the pressure setting matches the viscosity of the solution being administered, as excessive force can cause tissue irritation or aspiration hazards. Additionally, the device should never be shared between patients unless it has undergone complete reprocessing according to manufacturer guidelines. Regular inspection for cracks, leaks, or wear is mandatory to guarantee optimal performance. Improper storage in humid environments may degrade internal seals, compromising functionality. By following these operational standards, medical staff can maximize therapeutic efficacy while minimizing adverse events. This tool remains an indispensable asset in modern respiratory and ENT care, bridging the gap between effective drug delivery and patient comfort through its reliable engineering and user-centric design.