Bio Medical Waste Incinerator and Unwanted materials generated by human activities from Residential, Commercial and Industrial areas in Towns and Metro Cities
payment terms ( 100-1000 units 100% advance payment ) ( 1000-10000 units 50% advance payment after contract and 50% before shipping ) thanks for your cooperation.
BPAP Systems are Bi-level PAP (Bi-level Positive Airway Pressure) devices intended to provide non-invasive ventilation for patients with Obstructive Sleep Apnea (OSA) and Respiratory Insufficiency. They are intended for adult patients by prescription in the home or hospital/institutional environment. With its Target Tidal Volume function and other excellent comfort features and effective performance, it offers each patient personalized ventilation support.
IPhAPPa:4 -30 hPa
EPAP:4-25EPhAPPa:4-25hPa 3.5-inch 3.5-inch CPA
Y-30T
CPAP modeC:P4A-P20mhoPdae:4-20hPa
P , S , T ,CSP/TA P , S , T , S /T
This kit is used for the qualitative determination of COVID-19 IgM/IgG antibodies in human serum, plasma and venous whole blood samples in vitro. as an auxiliary diagnosis of COVID-19 infection.
[Detection principle]
This kit uses colloidal gold immunochromatography. Testing COVID-19 IgG antibody and COVID-19 IgM antibody in human serum, plasma and whole blood samples. The blood samples diluent containing COVID-19 IgG antibody and/or COVID-19 IgM antibody chromatography to colloidal gold binding pad, recombinant with colloidal gold marked COVID-19 antigen antibody, forming colloidal gold - antigen complex, chromatography to test area, combining to precoated anti-human IgG antibody and/or anti-human IgM antibody respectively, forming complexes in the test area and presenting red precipitation line. Unbound rabbit IgG colloidal gold bond chromatography to quality control line (C) combined with precoated sheep anti-rabbit IgG antibody presented a red precipitation line.
If the samples do not contain COVID-19 IgG antibody and/or COVID-19 IgM antibody, there is no corresponding red precipitation line existed in the test area. A red precipitation line appears on the quality control line (C) no matter if there is COVID-19 IgG antibody and/or COVID-19 IgM antibody in the sample or not.
[Storage and Stablity]
1. Store at 2ï½?30 for 18 months in a cool place, no direct sunlight and no freeze preservation. The test card and sample diluent should be used up in 1 hour after opening the package (opening temperature 10~30, humidity 25%~95%).
2. The date of production and the term of use are labeled.
Muscle Stimulator is a computerized Diagnostic Stimulator unit with Therapeutic, Iontophoresis and TENS facility. Treatment mode, time and other parameters are displayed in the LCD, soft touch keys are used to select the modes and parameters. Digital display indicates the output current in mA. In IG mode Rectangular/ Triangular pulses can be selectable.
APPLICATION
To stimulate sensory and motor nerves, facilitate muscle contraction re-educate muscle, improve circulation, prevent/stretch adhesions, hypertrophy muscle, prevent contractures and to test muscle for enervation.
(IFT+TENS+MS+US) :Interferential therapy has its uses in pain relief and muscular contraction. It is used as a technique to achieve either of these when other methods are not appropriate or unavailable, and are often conducted in conjunction with other treatments.
Interferential therapy has its uses in pain relief and muscular contration. It is used as a technique to achieve either of these when other methods are not appropriate or unavailable, and are often conducted in conjunction with other treatments.
1. Medium concentration 2. With green elastic band (latex) 3. Adjustable nose clip
4. With 2m oxygen tube 5. Color: green transparent (face mask and hose) 6. Packing: 1 pc/plastic bag (with instruction label inside), 100 pcs/carton 7. Non-sterile
With these booths medical staff can be sure that they have protection from infectious diseases while undergoing testing activities. Each booth is prefabricated for easy installation and quick use at airports,
hospitals or other testing locations. There are two types available (stalls or
extended room) depending on the need and include speakers, microphones, gloves and pressure equipment
Canine Distemper Virus (CDV)/Canine Adenovirus (CAV)/Canine Influenza Virus (CIV) Ag Combo Test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for the rapid and qualitative detection of Canine Distemper, Virus, Canine Adenovirus and Canine Influenza Virus antigens in dog's nasal secretion
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