Описание Инфузионная система 22G представляет собой важный медицинский инструмент, применяемый для точного и безопасного введения инфузионных растворов в периферические вены пациентов. Ее использование становится неотъемлемой
O equipo de infusão por gravidade com gotejamento macrogotas, que permite a administração de 20 gotas por mililitro, juntamente com um conector Luer Slip, foi especificamente desenvolvido para facilitar a administração de medicamentos e soluções diretamente na corrente sanguínea do paciente.
A whole assembly process of an IV infusion set by machine, including the assembly of the fluid filter, the assembly of the drip chamber with spike, the assembly of the roller clamp, the assembly of the injection port, and the assembly of the IV tubing.
Here is the list of the IV set parts name: Protective cap, Plastic spike, Air vent cap& air filter, Drip chamber, Solution filter, Flow regulator: roller clamp, pinch clamp, slide clamp, and microflow regulator, Injection site: rubber tube or rubber bulb, Y injection site, Y needless connector, and drip chamber with the injection port, Luer connector: Luer lock connector and luer slip connector
Needle.
IV sets in Nigeria KY-RI-001 and KY-RI-004 IV sets are the most commonly used in Nigeria. The KY-RI-001 IV set has a vented spike with a
IV sets come in different sizes and configurations to meet each patient’s specific needs and treatment. The IV set size includes tubing length, needle size, macro
Inspecting the quality of IV sets based on physical properties can help ensure that they are safe and effective for use in medical treatment. Here are some aspects of inspecting IV set quality based on physical properties.
As a manufacturer, we have 30 years of professional production experience in China. Know more about us. The way to distinguish these two IV sets
Types based on applications Micro vs. Macro Micro IV set As the name implies, the micro IV set has a device with a narrower diameter in
Focus on the production of disposable infusion sets which meet the requirements of CE and ISO 13485 according to REGULATION (EU) 2017/745.
