Verathon is a medical device company that produces various products, including devices used in airway management and visualization.
Here are some general considerations based on the components mentioned:
Gliderite Rigid Stylet: A stylet is a rigid or flexible rod-like device that is often used to assist in the placement of various medical instruments, such as endotracheal tubes or other airway devices.
Verathon: Verathon's products are often related to airway management and medical imaging, so the Gliderite Rigid Stylet might be used in procedures involving airway management.
Applications: Rigid stylets are commonly used in the field of anesthesiology and emergency medicine to aid in the insertion of airway devices, ensuring proper placement and reducing the risk of complications.
An endobronchial tube is a medical device designed for use in the respiratory system, specifically within the bronchial tubes. These tubes are used in various medical procedures, such as bronchoscopy, endobronchial intubation, and lung surgery. The primary purpose of an endobronchial tube is to maintain an open airway and facilitate the delivery of oxygen or anesthesia to the patient's lungs during surgical or diagnostic procedures.
Key features and uses of endobronchial tubes include:
Bronchoscopy: Endobronchial tubes are often used in bronchoscopy procedures, allowing physicians to visually examine the bronchial tree and perform diagnostic or therapeutic interventions.
Lung Surgery: During certain lung surgeries, endobronchial tubes may be employed to isolate and collapse one lung, providing a clear field of view for the surgeon.
Ventilation: Endobronchial tubes can be used for selective lung ventilation. They can be positioned to direct ventilation to a specific lung, allowing the other lung to be collapsed or isolated.
Anesthesia: In some cases, endobronchial tubes are used for delivering anesthesia during thoracic surgeries or procedures.
Cordis is a well-known medical device company that produces a variety of products, including devices used in interventional cardiology and vascular procedures.
The Cordis Saber PTA balloon is likely designed for use in percutaneous transluminal angioplasty procedures. Angioplasty is a medical procedure used to open narrowed or blocked blood vessels, typically arteries, to improve blood flow. During angioplasty, a balloon catheter is inflated at the site of the blockage to widen the vessel and restore blood flow.
Here are some general features you might expect from a PTA balloon like Cordis Saber:
Balloon Material: The balloon is typically made of materials like polyethylene or polyurethane.
Inflation System: It would likely have an inflation system that allows controlled inflation and deflation of the balloon during the procedure.
Catheter Design: The balloon is mounted on a catheter, which is a flexible tube that allows the device to be threaded through blood vessels to the site of the blockage.
Guidewire Compatibility: PTA balloons are often designed to be used with guide wires for precise placement.
Refer Standards
ISO 9626: 1991 + AMENDMENT 1 2001 Stainless steel needle tubing for the manufacture of medical devices.
ISO 8537:2007 Sterile single-use syringes, with or without needle, for insulin.
ISO 10993-7:2008 Biological evaluation of medical devices - Part 7 : Ethylene oxide sterilization residuals.
ASTM F 1140/F 1140M-13 Standard test methods for internal pressurization failure resistance of unrestrained packages.
USP 37-NF 32 <85> Bacterial Endotoxins Limit.
ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Part 2: Test of sterility performed in the definition, validation and maintenance of a sterilization process.
ISO 11135-1:2007 Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices.
Refer Standards
EN ISO 8537:2007 Sterile single-use syringes, with or without needle, for insulin.
EN ISO 9626:1991 / AMD. 1: 2001 Stainless steel needle tubing for the manufacture of medical devices AMENDMENT 1.
ASTM F88/F88M-09 Standard Test Method for Seal Strength of Flexible Barrier Materials.
ASTM F1140/F1140M -13 Standard Test Methods for Internal Pressurization Failure Resistance of Unrestrained Packages.
ISO 10993-7:2008 Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals.
USP 37- NF32 2014: U.S. Pharmacopeia National Formulary.
