Medical Supplies

Product Description NEB-001 FDA approved Intelligent Mesh Nebulizer NEB-001 FDA approved Intelligent Mesh Nebulizer world’s first mobile game guided mesh nebulizer approved by FDA Feature 1. Small and portable,Only 100g,lighter than a smart phone. 2. Rechargeable and long duration. Built-in rechargable lithium battery provides 4-6 hours’ nebulization.Charging via a a USB port. 3. Whisper quitet, operation noise is less than 50dB,even quieter than whisper. 4. Adjustable strength of atomization via APP,3different levels of atomization rate(High-Middle-Low) are available. Ultrafine particles for better therapeutic effects NEB-001 has achieved, that more than 80% of particles during the nebulization treatment are smaller than 5µm, and the MMAD is only 2.2 µm. Medicine can DIRECTLY access at the affected area. NEB-001 Intelligent Mesh Nebulizer FDA Mesh Portable Nebulizer 0 Mobile Game App Guided Atomization via Bluetoot NEB-001 nebulizer can connect with a game app via Bluetooth, increasing the interest of treatment and enhancing compliance apparently. With rigorous design,the game encourages patients to take deep breath and finally increases the lung deposit of medicine. NEB-001 Intelligent Mesh Nebulizer FDA Mesh Portable Nebulizer 1 Original I.A.D Technology IAD technology is progressed by a smart respiratory sensor to realize "Respiratory Monitoring", which allows the nebuliz­er to atomize medicine while inhaling, and suspend atomizing while exhaling, reducing the feeling of cough. NEB-001 Intelligent Mesh Nebulizer FDA Mesh Portable Nebulizer 2 Specification Model Number NEB-001 Power Supply Lithium Battery Nebulization Rate ≥0.2mL/min Power Consumption ＜1.5 W MMAD 4.0μm±25% Working noise ≤40dB Medical Cup Volume 8mL Weight 100g±5g Dimensions 50mm(L)×79mm(W)×110mm(H) Nebulizer consumable accessories NEB-001 Intelligent Mesh Nebulizer FDA Mesh Portable Nebulizer 3 FAQ A: Are you factory or a trading company? Q: We are factory and we have our own R&D and QC team. A: What certificates do you have? Which markets can you you sell? Q: We have US FDA,CE certificates. We already sold our products in USA, Latin America,Europe, Asia,Middle East. A: Can you do the desire and custom work for me? Q: We can offer both OEM and ODM service according to customers’ request.

Feature Made of transparent soft PVC for good visualization. Provide various choice to suit different requirement: 24%(Blue),28%(Yellow), 31(White), 35%(Green), 40%(Pink),50%(Orange). Single venturi valve is available with fixed concentration. The standard length of tube is 2.1m,and different length is available. Venturi mask Oxygen concentration Oxygen flow Blue 24% Yellow 28% White 31% Green 35% Pink 40% Orange 50%

Detailed Product Description High Light: x ray mri x-ray film, medical imaging film 10in * 14in Digital x-ray Dry Medical Imaging Films For Thermal Printers KND-F Description: Konida Medical x-ray Dry Film (KND-A/F) Konida Medical x-ray Dry Film (KND-A/F) has image layer and protect layer on different side of bluish polyester bases, and there are no sensitive silver halide in both layer. The film is fit for thermal printer to print digital image which is processed and stored in the computer, to attain the enhanced x- ray image quality. Compared to traditional silver halide processing, the procedure is more convenient and the speed of processing is faster. Meanwhile, it reaches to the goal of environment protection because the whole procedure is free of the Chemicals. Features Low fog High sharpness High max density Bright tone Compatible with thermal printers. Safe light It can be processed under room light condition since the film is not sensitive to light. Processing The product can be directly printed with thermal printers to get ideal image. The print conditions should be tested when using in other printer types. Storage Please store the film in cool and dry place without dust. Keep away from direct sunlight, acid or alkaline gas. Details as follows 1. Temperature and humidity,temperature 10℃～23℃, humidity 30％～65％RH, keep away from the heat resource.2. Gas,There are no hydrogen sulfide, ammonia, sulfur dioxide, formaldehyde, and any other alkaline gas, etc. 3. Pile,Please keep film upright to avoid the bad influence caused by pressure. Period of validity The period of validity is 24 months under above conditions. Conditions of usage The best condition of usage as followingTemperature 18℃～24℃, humidity 50%～ 65%RH. Notes 1. Store the film under the conditions specified above. 2. Take the film out of the cool place and place the film with the package in the place where the film will be used for at least 4 hours, to avoid the steam concentrate on the film and damage the film. 3. It should be careful to handle the film, don’t crash, fold, distort and rub the film, don’t touch the film with wet hand. 4. Dealing with the waste film should obey the local law and regulations. Package and Size 1.Konida Medical film type, KND-A, Suitable for AGFA 5300,5302,5500,5502,3000. Name Model type Size Sheets/box Boxes/ca , se Konida medical dry film KND-A 8in×10in 20cm×25 , cm 100 5 10in×12in 25cm×30cm 100 5 11in×14in 28cm×35cm 100 5 14in×17in 35cm×43cm 100 5 2.Konida Medical film type, KND-F,suitable for Fuji 3000,2000,1000. Name Model type Size Sheets/box Boxes/ca , se Konida Medical dry film KND-F 8in×10in 20cm×25 , cm 100 5 10in×14in 28cm×35cm 100 5 14in×17in 35cm×43cm 100 5

A rapid test for the diagnosis of inflammatory condition by detecting CRP qualitatively in whole blood, serum or plasma CE certified Applications: The CRP Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of human CRP in whole blood, serum or plasma as an aid in the diagnosis of inflammatory condition. The cut-off of the test is 10 μg/ml. Description: C-reactive Protein (CrP) in patient’s sera has been found in association with acute infections, necrotic conditions and a variety of inflammatory disorders. There is a strong correlation between serum levels of CrP and the onset of the inflammatory process. Monitoring the levels of CrP in patient’s sera indicates the effectiveness of treatment and the assessment of patient recovery. It is used in particular to differentiate bacterial infections from virus infections. How to use? Bring tests, specimens, buffer, and/or controls to room temperature (15-30°C) before use. 1. Remove the Test Cassette from its sealed pouch, and place it on a clean, level surface. For best results, the assay should be performed within one hour. 2. Open the tube with the diluted sample .Transfer 3 drops(approximately 120µL)of mixed specimens to sample well. Start the timer. 3. Wait for the colored lines to appear. The result should be read at 5 minutes. Do not interpret the result at 10 minutes. CRP Rapid Test Cassette Diagnostic Blood Tests Rapid Chromatographic Immunoassay 0 INTERPRETATION OF RESULTS (Please refer to the illustration above) POSITIVE:* Two lines appear. One colored line should be in the control line region (C) and another apparent colored line should be in the test line region (T). *NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of CRP antigen present in the specimen. Therefore, any shade of color in the test line region (T) should be considered positive. NEGATIVE: One colored line appears in the control line region (C). No line appears in the test line region (T). INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue using the test kit immediately and contact your local distributor. NOTE: 1. The intensity of the color in the test region (T) may vary depending on the concentration of analytes present in the specimen. Therefore, any shade of color in the test region should be considered positive. Please note that this is a qualitatively test only, and cannot determine the concentration of analytes in the specimen. 2. Insufficient specimen volume, incorrect operating procedure or expired tests are the most likely reasons for control line failure.

The cannular shall be clean, straight and free of any dirt and sundries. After being lubricated, the lubricant shall not be visible as droplets of fluids on the outside or inside surface of the needle tube, the hub shall be free of obvious flash, bur, bubble and any other injectiong defects, the needle tube and hub shall be bonded straight. The assembly hole of the needle hub shall be free of particles and dirt and the needle tip shall be free of any but and hook.

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