Foam cervical collars The foam cervical collars specification as following, Shaped for comfort and to give the correct support to help relieve the pain suffered from whiplash, stiff neck and muscular tension. Made from high density closed cell foam (100D) for better support, have a woven covering. Available in 3 sizes; small, medium and large. Small: Length 44cm; Width: 9cm; Medium: Length 48cm; Width: 10cm; Large: Length 53cm; Width: 11cm
Hyden specimen bottle (Male and or Female) HYDEN Specimen bottles 60ml Polyethylene Terephthalate Bottle w/ Peach Pink or Aqua green Polypropylene Cap and Label Sticker 672 pcs per box
Hyden specimen bottle 60ml Polyethylene Terephthalate Bottle Color Coded Polypropylene Cap and Label Sticker Packing Corrugated Cartoon Box Weight Bottle-8.2 grams, Cap-3grams Cubic Meter
IV Cannula IV Cannula (all guage i.e 16, 18, 20,22 & 24 Gauge) and also ERECT IV CANNULA PROJECTS. Standard packing
Transfusion medical disposable product
IV cannulas IV cannula with wings with port g-16 to g-22 gauge Blister packing with 100 pcs per inner box . & 10 inner box consist of 1 outer box
Finest quality x-ray film chemical of international standards For all tanks sizes e.g. 1,2,3,5 Gallons
Mediflon size - 14,16,17,18,20,22,24g (IV Cannulae with injection valve and wings) Gross wt. 6.70 Volume wt. 7.008 Volume- 0.042cbm
Surgical blade Made of carbon steel/stainless steel Packed in aluminum foil Box of 100 pcs
Plastic dropper pack Manufactured using American jomar injection blow molding process in a clean room environment and conforms to pharma standards. Set comprises of bottle, nozzle and a cap Pack consists of two system 1. With open nozzle and a tamperevident cap in which case end user have just to open the pilferproof cap and dispence the medication 2. Blocked nozzle with a cap to pierce the blocked nozzle just before usage Sizes ranges from 5,10,15ml to 500ml. One carton consists of 2000 sets fo bottle, nozzle and cap. The gross wt of the 2000 sets with the carton is approximately 12kg.
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"Factview Urine Strip Glucose & Protein 2P" likely refers to a specific product or brand of urine test strip used for the qualitative detection of both glucose and protein in urine samples. These urine test strips are commonly used in healthcare settings for routine urinalysis to screen for various substances, including glucose and protein, which can indicate various health conditions when present in abnormal levels. Here's how they typically work: Sample Collection: A urine sample is collected from the patient. This sample is usually collected in a clean container and may be collected at any time of the day. Dipping the Strip: The urine test strip is dipped into the urine sample for a few seconds, ensuring that all the reagent pads on the strip are fully immersed in the urine. Reaction with Glucose and Protein: If glucose and protein are present in the urine sample, they will react with the respective reagents on the strip. This reaction typically produces color changes on the reagent pads corresponding to the concentrations of glucose and protein in the urine. Interpretation of Results: After a specified reaction time (usually a few minutes), the color changes on the reagent pads are compared to a color chart provided by the manufacturer. This chart helps determine the approximate concentrations of glucose and protein in the urine sample. A "Glucose & Protein 2P" urine strip indicates that it is specifically designed to detect both glucose and protein in urine and may have two separate pads (2P) for detecting each substance. These strips are useful for screening for conditions such as diabetes mellitus (glucose) and kidney disease or urinary tract infections (protein), where abnormal levels of these substances may be present in the urine. It's important to note that urine testing using test strips provides qualitative results and may not be as accurate as laboratory-based quantitative measurements of glucose and protein levels in urine. Therefore, any abnormal results obtained using urine test strips should be confirmed with further diagnostic tests for accurate diagnosis and management.
These urine test strips are commonly used in healthcare settings, including clinics, hospitals, and laboratories, as well as for at-home testing purposes. They are designed to provide a quick and convenient method for screening for various substances, including glucose, in urine. Here's how they typically work: Sample Collection: A urine sample is collected from the patient. This sample is usually collected in a clean container and may be collected at any time of the day. Dipping the Strip: The urine test strip is dipped into the urine sample for a few seconds, ensuring that all the reagent pads on the strip are fully immersed in the urine. Reaction with Glucose: If glucose is present in the urine sample, it will react with the reagent on the strip. This reaction typically produces a color change on the reagent pad corresponding to the concentration of glucose in the urine. Interpretation of Results: After a specified reaction time (usually a few minutes), the color changes on the reagent pads are compared to a color chart provided by the manufacturer. This chart helps determine the approximate concentration of glucose in the urine sample. A "Glucose 1P" urine strip may indicate that it is specifically designed to detect glucose in urine and may have a single pad (1P) for detecting glucose. These strips are useful for screening for conditions such as diabetes mellitus, where elevated levels of glucose may be present in the urine. It's important to note that urine glucose testing using test strips provides qualitative results and may not be as accurate as laboratory-based quantitative measurements of glucose levels in blood. Therefore, any abnormal results obtained using urine test strips should be confirmed with further diagnostic tests, such as blood glucose measurement, for accurate diagnosis and management.
Disposable adhesive cardiac electrode pads are medical devices used in electrocardiography (ECG) procedures to detect and record the electrical activity of the heart. Here's more information about these pads: Purpose: The primary purpose of disposable adhesive cardiac electrode pads is to securely attach ECG electrodes to the patient's skin, allowing for the acquisition of clear and accurate ECG signals. These pads serve as the interface between the patient's body and the ECG monitoring equipment. Design: Disposable adhesive cardiac electrode pads are typically made of soft, flexible material, such as foam or fabric, with an adhesive backing that adheres to the patient's skin. They are designed to be comfortable for the patient while ensuring reliable electrode contact and signal transmission. Electrode Placement: Disposable electrode pads are pre-gelled with conductive gel to ensure good electrical conductivity between the skin and the electrodes. They are usually pre-positioned on a backing material or individually packaged for easy application to specific locations on the patient's body, such as the chest, limbs, or torso. Adhesive Properties: The adhesive backing of the electrode pads is formulated to adhere securely to the skin without causing discomfort or irritation. It should provide strong adhesion throughout the duration of the ECG procedure, even during patient movement or perspiration. Compatibility: Disposable adhesive cardiac electrode pads are compatible with various types of ECG machines and monitoring equipment, including 3-lead, 5-lead, and 12-lead ECG systems. They are suitable for use in hospitals, clinics, ambulances, and other healthcare settings. Disposable: As indicated by their name, disposable adhesive cardiac electrode pads are intended for single-use only. After the ECG procedure is complete, the pads are removed from the patient's skin and discarded according to medical waste disposal protocols. Hygiene: Disposable electrode pads help maintain hygiene and reduce the risk of cross-contamination between patients. They should be stored in a clean and dry environment before use, and proper hand hygiene practices should be observed when applying and removing the pads.
Aqua gel, also known as ultrasound gel or coupling gel, is a specialized gel used as a medium to transmit ultrasound waves between the transducer probe and the patient's skin during various medical imaging procedures such as ultrasound imaging (USG), cardiotocography (CTG), and fetal Doppler monitoring. Here's more information about aqua gel for USG, CTG, and fetal Doppler: Purpose: The primary purpose of aqua gel is to serve as a conductive medium that facilitates the transmission of ultrasound waves between the ultrasound probe and the patient's skin. This allows for the production of high-quality ultrasound images and accurate Doppler signals during imaging and monitoring procedures. Composition: Aqua gel is typically water-based and contains ingredients that provide viscosity, lubrication, and acoustic coupling properties. Common ingredients may include water, glycerin, propylene glycol, cellulose derivatives, preservatives, and sometimes colorants or fragrances. Conductivity: Aqua gel is formulated to have optimal acoustic properties, ensuring efficient transmission of ultrasound waves while minimizing air pockets or impedance that could degrade image quality or Doppler signals. High-quality aqua gel ensures clear visualization of anatomical structures and accurate assessment of blood flow. Viscosity: The gel's viscosity is designed to be suitable for easy application and spreadability on the skin without dripping or running. It should provide sufficient contact between the ultrasound probe and the skin surface while allowing for smooth movement during scanning. Non-Irritating: Aqua gel is typically formulated to be hypoallergenic, non-greasy, and non-irritating to the skin. It should be gentle and comfortable for patients, even those with sensitive skin, to ensure a positive imaging or monitoring experience. Compatibility: Aqua gel is compatible with a wide range of ultrasound transducers and probes used in various medical imaging applications, including abdominal, obstetric, vascular, cardiac, and musculoskeletal ultrasound examinations. It is suitable for use with both standard and specialized ultrasound equipment. Application: Before applying aqua gel, the skin should be cleaned to remove any oils, lotions, or dirt that may interfere with ultrasound transmission. A generous amount of gel is then applied to the skin at the imaging or monitoring site before placing the ultrasound probe or Doppler transducer. Hygiene: Aqua gel should be stored in a clean and dry environment to prevent contamination. Single-use disposable packets or bottles with dispensing caps are commonly used to maintain hygiene and prevent cross-contamination between patients.
Tear Test Strips, specifically those of the Schirmer type, are diagnostic tools commonly used in ophthalmology to measure tear production. Here's more information about Tear Test Strips of the Schirmer type: Purpose: Tear Test Strips (Schirmer) are primarily used to assess the quantity of tears produced by the lacrimal glands. This test helps diagnose conditions such as dry eye syndrome, also known as keratoconjunctivitis sicca, by evaluating tear production levels. Design: Schirmer Tear Test Strips are thin, paper-like strips that are usually marked with millimeter (mm) gradations. The strips are typically designed to be inserted into the lower eyelid's conjunctival sac, where they absorb tears over a specified period. Packaging: Tear Test Strips (Schirmer) are commonly packaged in individual packets or vials to maintain sterility and prevent contamination. A pack of 100 Tear Test Strips would contain 100 individual strips, each sealed in its own packet. Usage: To perform the Schirmer Tear Test, a single strip is inserted into the lower eyelid's conjunctival sac, usually at the outer corner of the eye. The patient is instructed to keep their eyes closed during the test, which typically lasts for a few minutes. After the specified time, the strips are removed and the amount of tear wetting is measured using the mm gradations on the strip. Interpretation: The length of tear wetting on the Tear Test Strip (Schirmer) provides an indication of the quantity of tears produced by the lacrimal glands. Reduced tear wetting may indicate decreased tear production, which can be indicative of dry eye syndrome or other ocular surface disorders. Variations: There are variations of the Schirmer Tear Test, including the Schirmer I test (without anesthesia) and the Schirmer II test (with anesthesia). The Schirmer I test measures basal tear secretion, while the Schirmer II test evaluates reflex tear secretion after instillation of anesthetic eye drops. Safety and Precautions: Tear Test Strips (Schirmer) should be handled and disposed of according to standard precautions for ocular diagnostic procedures. Care should be taken to avoid contamination and ensure accurate test results.
Tear Test Strips, commonly used in ophthalmology, are diagnostic tools to assess tear production and the health of the ocular surface. Here's more information about Tear Test Strips with Rose Bengal dye: Purpose: Tear Test Strips with Rose Bengal dye are primarily used to evaluate tear production and diagnose conditions such as dry eye syndrome, keratoconjunctivitis sicca, and other ocular surface disorders. Rose Bengal dye stains areas of the ocular surface where there is damage or insufficient tear film, aiding in the diagnosis of these conditions. Composition: Tear Test Strips with Rose Bengal dye are thin, paper-like strips impregnated with Rose Bengal dye. Rose Bengal is a water-soluble stain that binds to damaged or devitalized cells on the ocular surface, highlighting areas of dryness, inflammation, or epithelial defects. Packaging: Tear Test Strips are typically packaged in individual packets or vials to maintain sterility and prevent contamination. A pack of 100 Tear Test Strips would contain 100 individual strips, each sealed in its own packet. Color: Tear Test Strips with Rose Bengal dye often have a distinctive pink or red color due to the presence of the dye. This coloration facilitates visualization and interpretation of the staining patterns on the ocular surface. Usage: To perform a Tear Test, a single strip is moistened with a sterile saline solution or artificial tears and then gently applied to the lower eyelid margin of the patient's eye. After a specified time, usually around 15-30 seconds, the strip is removed, and the staining pattern on the ocular surface is evaluated under a slit lamp or other magnification device. Interpretation: Areas of the ocular surface that are stained with Rose Bengal dye indicate regions of compromised epithelial integrity, reduced tear film stability, or inflammation. The severity and extent of staining can provide valuable information about the underlying pathology and guide treatment decisions. Safety and Precautions: Tear Test Strips with Rose Bengal dye should be handled and disposed of according to standard precautions for ocular diagnostic procedures. Care should be taken to avoid contact with the patient's skin and mucous membranes, and any unused strips should be discarded after use.