FEATURES: DIN rail mounting for easy installation Plug connectors for quick and easy connection or rewiring 25kA Iimp capability Thermal disconnect device Status indicators visually verify protection level Surge protection device with N-PE residual current spark gap as 3+1 circuit Remote alarm function ISO 9001ï¼?2008 certificatedï¼?ISO14000:2004 certificated and OHSAS18000ï¼?2007 certificated High quality products with CE, Rohs certificates
As the world's largest condom maker, we also manufacture personal lubricants. We manufacture latex condoms that are made from premium quality natural rubber latex. Our condoms are designed with total reliability whereby each condom is electronically tested to provide maximum protection and safety. Every design is carefully engineered by our Research and Development team which comprises of industry experts and each variant is developed to create the ultimate pleasure and safety for consumers. All our lubricants are Class IIa medical devices which comply with the new EU MDR regulations in force since May 2021. Medical Device ingredients are pharmaceutical grade, whereas non-medical / cosmetic lubricants have no restrictions. All our lubricants are compatible with latex condoms and are all 100% paraben free. Our personal lubricants can be used up to 6 months after opening. Our personal lubricants also meet the stringent harmonized standards such as ASTM D7661, NF97-034 and the WHO guidelines. *MOQ Condoms from 3000 gross * MOQ Lubes from 10000 Tubes/bottles
The "SpiderFX" may refer to a specific type of embolic protection device used during carotid artery stenting procedures. Embolic protection devices are designed to capture and remove debris released during the stenting process to prevent it from traveling to the brain, reducing the risk of stroke.
The EV3 SpiderFX is commonly associated with the SpiderFX Embolic Protection Device, which is used in the field of interventional cardiology. The device is designed to capture and remove embolic debris that may be released during certain vascular procedures, particularly during carotid artery stenting. Key features of the EV3 SpiderFX Embolic Protection Device may include: Embolic Protection: The primary function of the device is to provide protection against embolic debris dislodged during the intervention. It helps prevent these debris from reaching and potentially blocking smaller blood vessels. Flexible Design: The SpiderFX typically has a flexible design that allows it to navigate through blood vessels, facilitating the deployment and retrieval process. Distal Protection: The device is designed to be positioned distal to the treatment site, capturing any embolic debris before it can travel downstream. Capture Basket: The device often includes a capture basket that traps and retains embolic debris, preventing it from causing harm in the circulation. Compatibility: The SpiderFX device is designed for compatibility with various catheters and guide wires commonly used in interventional procedures.
Safety Huber Needle Features and Benefits Sterile pack, single use only. Needle-stick prevention, safety assured. Special needle tip design to prevent rubber fragment contamination. Luer connector, equipped with needleless connector, heparin cap, Y three-way. Chassis sponge design for a more comfortable application. High pressure resistant central line with 325 P.S.I Two holes connector optional. MDR 2017/745 USA FDA 510K Refer Standards ISO 10555-6:2015 Intravascular catheters - Sterile and single-use catheters Part 6: Subcutaneous implanted ports. ISO 8536-4: 2010 Infusion equipment medical use- Part 4: Infusion Sets for single use, gravity feed. ISO 23908:2011 Sharps injury protection Requirements and test methods - Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood Samplings. ISO 7864:2016 Sterile Hypodemic Needles for Single-use requirements and test methods. ISO 9626:2016 Stainless Steel Needle Tubing for the Manufacture of Medical Devices requirements and Test methods. ISO 80369-7: 2016 Small - bore connectors for liquids and gases in healthcare applications. Part 7: Connectors for intravascular or hypodermic applications. ISO 10993-7:2008 Biological Evaluation of Medical Device - Part 7: Ethylene Oxide Sterilization Residuals.
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