1. INTENDED USE CPV + CCV +Giardia Ag Triple Test is a combined cassette to differentially diagnose the presence of Canine Parvovirus antigen, Canine Coronavirus antigen and Giardia antigen in dogâ??s feces or vomit. Assay Time: 5-10 min Sample: Feces or vomit 2. PRINCIPLE OF THE ASSAY CPV + CCV + Giardia Ag Triple Test is based on sandwich lateral flow immunochromatographic assay. The test device has three testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough CPV antigen, CCV antigen or Giardia antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CPV, CCV or Giardia antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches, each containing onecassette and a desiccant - 10Ã?assay buffer tubes (1.0 mL each) - 10Ã?pipettes - 10Ã?swab sticks - Product Manual
1. INTENDED USE CPV + CCV Ag Combined Test is a combined cassette to differentially diagnose the presence of Canine Parvovirus antigen and Canine Coronavirus antigen in dogâ??s feces or vomit. Assay Time: 5 -10 min Sample: Feces or vomit 2. PRINCIPLE OF THE ASSAY CPV + CCV Ag Combined Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough CPV antigen or CCV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CPV antigen or CCV antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches, each containing acassette, pipette and desiccant - 10Ã?assay buffer tubes (1.0 mL each) - 10Ã?swab sticks - Product Manual
Feline Leukemia Test INTENDED USE Feline Leukemia Virus AG Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Leukemia Virus antigen in cat's blood. Assay Time: 5-10 min Sample: Serum,Plasma or Whole Blood Feline Leukemia Test PRINCIPLE Feline Leukemia Virus AG Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough feline leukemia virus antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of feline leukemia virus antigen in the sample. Feline Leukemia Test KIT COMPONENT 1. Foil pouches, each containing one cassette, one pipette and a desiccant 2. Assay buffer (2.0 mL) 3. Centrifugal tubes 4. Product Manual Feline Leukemia Test TEST PROCEDURE 1. Take cat's blood, serum or plasma as sample. 2. Take out the cassette from the foil pouch and place it horizontally. 3. Drip 1 drop of sample and immediately drip 2 - 3 drops of assay buffer into the sample hole "S". 4. Interpret the result in 10-15 minutes. Result after 15 minutes is considered as invalid.
Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
Specimen:Whole Blood /Serum / Plasma D-Dimer Rapid Test Device is used for the qualitative detection of D-dimer in human whole blood and plasma; The test is used as an aid in the assessment and evaluation of patients with suspected disseminated intravascular coagulation (DIC), deep vein thrombosis (DVT), and pulmonary embolism (PE). During blood coagulation process, fibrinogen is converted to fibrin by the activation of thrombin. The resulting fibrin monomers polymerise to form a soluble gel of non-cross-linked fibrin. This fibrin gel is then converted to cross-linked fibrin by thrombin activated Factor XIII to form an insoluble fibrin clot. Production of plasmin, the major clot-lysing enzyme, is triggered when a fibrin clot is formed. Although fibrinogen and fibrin are both cleaved by the fibrinolytic enzyme plasmin to yield degradation products, only degradation products from cross-linked fibrin contain D-dimer and are called cross-linked fibrin degradation products. Therefore, fibrin derivatives in human blood or plasma containing D-dimer are a specific marker of fibrinolysis. The D-Dimer Rapid Test Device (Whole blood//Plasma) detects D-Dimer through visual interpretation of color development in the internal strip. Anti-D-Dimer antibodies are immobilized on the test region of the membrane, and anti-mouse antibodies immobilized on the control region. During testing, the specimen reacts with anti-D-Dimer antibodies conjugated to colored particles and precoated onto the sample pad of the strip. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient D-Dimer in the specimen, a colored band will form at the test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
One-Step Adenovirus Ag Rapid Test Formats:Uncut Sheets , Bulk Package, 30Tests/Box ,OEM Specimen:Feces INTENDED USE The Adenovirus Rapid Test Device (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of adenovirus in human fecal specimens. This kit is intended to be used as an aid in the diagnosis of adenovirus infection. INTRODUCTION Acute diarrheal disease in young children is a major cause of morbidity worldwide and is a leading cause of mortality in developing countries. Research has shown that enteric adenoviruses, primarily Ad40 and Ad41, are a leading cause of diarrhea in many of these children, second only to the rotaviruses. These viral pathogens have been isolated throughout the world, and can cause diarrhea in children year round. Infections are most frequently seen in children less than two years of age, but have been found in patients of all ages. Further studies indicate that adenoviruses are associated with 4-15% of all hospitalized cases of viral gastroenteritis. Rapid and accurate diagnosis of gastroenteritis due to adenovirus is helpful in establishing the etiology of gastroenteritis and related patient management. Other diagnostic techniques such as electron microscopy (EM) and nucleic acid hybridization are expensive and labor-intensive. With the self-limiting nature of adenovirus infection, such expensive and labor-intensive tests may not be necessary.
The Chagas Ab Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgG anti-Trypanosoma cruzi (T. cruzi) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with T. cruzi. Any reactive specimen with the Chagas Ab Rapid Test must be confirmed with alternative testing method(s) and clinical findings. Chagas disease is an insect-borne, zoonotic infection by the protozoan T. cruzi, which causes a systemic infection of humans with acute manifestations and long term sequelae. It is estimated that 16-18 million individuals are infected worldwide, and roughly 50,000 people die each year from chronic Chagas disease (World Health Organization)1. Buffy coat examination and xenodiagnosis used to be the most commonly methods2,3 in the diagnosis of acute T. cruzi infection. However, both methods are either time consuming or lack of sensitivity. Recently, serological test becomes the mainstay in the diagnosis of Chagasâ??s disease. In particularly, recombinant antigen based tests eliminate false-positive reactions which are commonly seen in the native antigen tests4-5. The Chagas Ab Rapid Test is an instant antibody test which detects IgG antibodies the T. cruzi within 15 minutes without any instrument requirements. By utilizing T. cruzi specific recombinant antigen, the test is highly sensitive and specific.
INTENDED USE The neisseria gonorrhoeae antigen test card is a rapid visual immunoassay for the qualitative detection of neisseria gonorrhoeae in female endocervical swab and male urethral swab specimens. This kit is intended for use as an aid in the diagnosis of neisseria gonorrhoeae infection. PRINCIPLE The neisseria gonorrhoeae antigen test kit is designed to detect N. Gonorrhoeae through visual interpretation of the color development in the internal strip. The membrane was immobilized with gonococcal Antigen-specific polychonal antibody on the test region (T) and related antibodies on the control region(C). During testing, the specimen is added to the sample region (S) and reacts with anti-gonococcus antibodies conjugated to colored particles and precoated onto the sample pad of the test. Then, the mixture migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient gonococcus antigens in the specimen, a colored band will form at the test region (T) of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
INTENDED USE The One Step RV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Rubella (Virus) in Whole Blood /Serum / Plasma to aid in the diagnosis of RV infection. The test is based on immunochromatography and can give a result within 15 minutes. PRINCIPLE The One Step RV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of RV antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing RV recombinant envelope antigens conjugated with Colloid gold (RV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-RV, T2 band is coated with antibody for the detection of IgG anti-RV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-RV, if present in the specimen, will bind to the RV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a RV IgG positive test result and suggesting a recent or repeat infection. IgM anti-RV if present in the specimen will bind to the RV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a RV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
A mesh nebulizer for aerosol drug deliverypowered by the latest vibrating mesh technologythat can use anywhere and any time. The mesh disc is made of 316 stainless steel and was perforated with more than 1200 precision formed holes (m) Electricity (approx. 130KHz) vibrates the mesh to make medication into very small particles (MMAD 1-5m) which come out of the mesh and form very fine mist for user inhalation.
Emergency and transport ICU grade electronic ventilator Features Vt range: 20-2000ml(VCV);Applicable to adult, pediatric infant(â?¥5Kg) Ventilation modes: A/C(V),A/C(P),SIMV(V)+PS,SIMV(P)+PS,SPONT,PRVC 8.4 inch LCD screen for easy observation Touch screen & Navigation knob for simple operation Simultaneous display of 3 waveforms and 2 loops Synchronized nebulizer(optional) Expiratory valve is autoclavable to avoid cross-infection Active exhalation valve with anti-condensation design World leading brands of key components of ventilator ensure high accuracy and stable performance Advanced proportional solenoid technology to realize accurate ventilation control Multi-safety mechanism and three-priority alarm of visual and audio for different risks
Vt range: 20-2000ml; Applicable to adult, pediatric and infant Ventilation modes: VCV, PCV, SIMV(P)+PS, SIMV(V)+PS, SPONT/CPAP, Sigh, PRVC, DualPAP, NPPV, Manual, Standby Weaning parameter ( RSB, P0.1, NIF) 15 inch TFT touch screen & big front view for easy observation Simultaneous display of 4 waveforms and 2 loops CO2 and SpO2 monitoring (optional) Synchronized nebulizer and air compressor (optional) Expiratory valve could be taken off for autoclavable disinfection to avoid cross-infection Active exhalation valve with anti-condensation design World leading brands of key components of ventilator ensure high accuracy and stable performance Advanced proportional solenoid technology realize accurate ventilation control Multi-safety mechanism and three-priority alarm of visual and audio for different risks
Model Number: OCE-ESWT-003; 1.Technical specification: (1)Display Screen: OLED display; (2)Control: operate on the handle directly without foot pedal; (3)Energy Level: 10 to 185 mJ (equivalent to 0.1~5 bar); (4)Operating Frequency: 1~22 Hz; (5)Treatment program: View all setup and treatment information on the phone via Bluetooth; (6)Service life of handle: 4 million shocks; 2.Feature: (1)No air compressor, no foot pedal, portable design and low maintenance cost; (2)Small volume-1/3 of portable type; (3)Complete functions-almost the same as the portable type; (4)Easy to control-no foot switch, operate on the handle directly; (5)Modern look-the smallest one; (6)Bluetooth 4.0 communication function-connect with smart device; (7)APP on Android and IOS; (8)Build-in user platform; 3.Package information: (1)Dimension: 300*240*180mm(L/W/H, the device); (2)Weight: 6Kg (the device); (3)Package: inside aluminum alloy case, outside carton; 4.Warranty: 3 years for the controller unit, 1 year for the accessories. 5.Certificates: CE, ISO 13485, FDA 6.Applications: (1)Physiotherapy; (2)Rehabilitation; (3)Orthopedics; (4)Sports medicine; (5)Aesthetic medicine; (6)ED treatment; (7)Treatment for urological pain and erectile dysfunction;
Work principle: Compressor free ballistic radial shock wave therapy system with electromagnetic generator as projectile accelerator. The hand piece contains a projectile that is accelerated through the electromagnetic transfer of kinetic energy. This kinetic energy is then transformed into impact energy in the applicator head. The impact energy delivered from the applicator head results in radial pulse in the target tissue. Technical specification: Model Number OCE-ESWT-002 Brand name Oceanus / OEM Instrument classification Class II Supply Ability 100 Unit/Units per Month Display Screen 7 inch LCD color touch screen Energy Level 10 to 185 mJ (equivalent to 0.1~5 bar) Operating Frequency 1~22 Hz Operating mode 4 Burst Mode (continuous/4/8/12 shocks) Preset treatment program 7 Preset treatment program Treatment site proposal More than 25 preset treatment recommendations Input voltage 100/240V AC Power Consumption 100/240VAC 50/60 Hz,250VA Fuse wire 250V/10A Service life of handle Minimum 4 million shocks Work enviroment requires 20 ºC -32 ºC 25% -75% RH 700hPa-1060hPa Storage environment requires 0 ºC -40 ºC 10% -93% RH 700hPa-1060hPa Transportation environment requires 10 ºC-70 ºC, 10% -93% RH, 700hPa-1060hPa Feature: *Ergonomic design provides a convenient setting operation *7 inch Display English touch screen design, intuitive *Imported power source, ensuring instant impact output effect *Wide impact pressure and frequency selection , in line with the demand for treatment *Single and dual output options, and offers a variety of specialty probes *7 preset treatment programme , adjustable *Non-invasive completely and no reported side effects, no hospitalization required *No air compressor, portable design and low maintenance cost List of the accessories: Object Quantity Host 1 Therapeutic handle 1 Foot switch 1 Therapeutic head Diameter of 6/15/25mm each 1 Power line 1 Handle pedestal 1 Handwriting pen 1 Silicone cap 10 Aluminum alloy suitcase 1 Product manual 1 Package information: *Dimension: 290*240*130(L/W/H, the host) *Weight: 2.07Kg (the host) *Package method: carton, there is also a aluminum alloy case package inside Warranty: 3 years for the controller unit, 1 year for the accessories. Clinical effect: *Body shapingAnti-cellulite treatment *Scar and wrinkle smoothing *Skin elasticity improvement *Connective tissue tightening *Treatment of pregnancy stretch marks *Treatment of post-liposuction irregularities Applications: *Physiotherapy *Rehabilitation *Sports medicine *Orthopedics *Aesthetic medicine *Treatment for urological pain therapy and erectile dysfunction Demo vedio of the shockwave therapy device: https://www.youtube.COM/watch?V=xu7Tbmr9dl4 Certificates: CE FDA ISO13485
Work principle: Compressor free ballistic radial shock wave therapy system with electromagnetic generator as projectile accelerator. The hand piece contains a projectile that is accelerated through the electromagnetic transfer of kinetic energy. This kinetic energy is then transformed into impact energy in the applicator head. The impact energy delivered from the applicator head results in radial pulse in the target tissue. Technical specification: Model Number OCE-ESWT-002 Brand name Oceanus / OEM Instrument classification Class II Supply Ability 100 Unit/Units per Month Display Screen 7 inch LCD color touch screen Energy Level 10 to 185 mJ (equivalent to 0.1~5 bar) Operating Frequency 1~22 Hz Operating mode 4 Burst Mode (continuous/4/8/12 shocks) Preset treatment program 7 Preset treatment program Treatment site proposal More than 25 preset treatment recommendations Input voltage 100/240V AC Power Consumption 100/240VAC 50/60 Hz,250VA Fuse wire 250V/10A Service life of handle Minimum 4 million shocks Work enviroment requires 20 ºC -32 ºC 25% -75% RH 700hPa-1060hPa Storage environment requires 0 ºC -40 ºC 10% -93% RH 700hPa-1060hPa Transportation environment requires 10 ºC-70 ºC, 10% -93% RH, 700hPa-1060hPa Feature: *Ergonomic design provides a convenient setting operation *7 inch Display English touch screen design, intuitive *Imported power source, ensuring instant impact output effect *Wide impact pressure and frequency selection , in line with the demand for treatment *Single and dual output options, and offers a variety of specialty probes *7 preset treatment programme , adjustable *Non-invasive completely and no reported side effects, no hospitalization required *No air compressor, portable design and low maintenance cost List of the accessories: Object Quantity Host 1 Therapeutic handle 1 Foot switch 1 Therapeutic head Diameter of 6/15/25mm each 1 Power line 1 Handle pedestal 1 Handwriting pen 1 Silicone cap 10 Aluminum alloy suitcase 1 Product manual 1 Package information: *Dimension: 290*240*130(L/W/H, the host) *Weight: 2.07Kg (the host) *Package method: carton, there is also a aluminum alloy case package inside Warranty: 3 years for the controller unit, 1 year for the accessories. Clinical effect: *Body shapingAnti-cellulite treatment *Scar and wrinkle smoothing *Skin elasticity improvement *Connective tissue tightening *Treatment of pregnancy stretch marks *Treatment of post-liposuction irregularities Applications: *Physiotherapy *Rehabilitation *Sports medicine *Orthopedics *Aesthetic medicine *Treatment for urological pain therapy and erectile dysfunction Demo vedio of the shockwave therapy device: https://www.youtube.COM/watch?V=xu7Tbmr9dl4 Certificates: CE FDA ISO13485
Work principle: Compressor free ballistic radial shock wave therapy system with electromagnetic generator as projectile accelerator. The hand piece contains a projectile that is accelerated through the electromagnetic transfer of kinetic energy. This kinetic energy is then transformed into impact energy in the applicator head. The impact energy delivered from the applicator head results in radial pulse in the target tissue. Technical specification: Model Number OCE-ESWT-003 Brand name Oceanus / OEM Instrument classification Class II Supply Ability100 Unit/Units per Month Display ModeOLED display Energy Level 10 to 185 mJ (equivalent to 0.1~5 bar) Pressure Range0.1~5 bar Operating Frequency1~22 Hz Input voltage100/240V AC Power Consumption100/240VAC 50/60 Hz,250VA Fuse wire 250V/10A Service life of handle Minimum 4 million shocks Work enviroment requires 20 ºC -32 ºC 25% -75% RH 700hPa-1060hPa Storage environment requires 0 ºC -40 ºC 10% -93% RH 700hPa-1060hPa Transportation environment requires 10 ºC-70 ºC, 10% -93% RH, 700hPa-1060hPa Feature: *Small volume-1/3 of portable type *Complete functions-almost the same as the portable type *Easy to control-no foot switch, operate on the handle directly *Modern look-the smallest one *Bluetooth 4.0 communication function-connect with smart device *APP on Android and IOS *Build-in user platform List of the accessories: Object Quantity Host 1 Therapeutic handle 1 Therapeutic head Diameter of 6/15/25mm each 1 Power line 1 Silicone cap 10 Aluminum alloy suitcase 1 Product manual 1 Package information: *Dimension: 300*240*180mm(L/W/H, the device) *Weight: 6Kg (the device) *Package method: carton, there is also a aluminum alloy case package inside Warranty: 3 years for the controller unit, 1 year for the accessories. Clinical effect: *Body shapingAnti-cellulite treatment *Scar and wrinkle smoothing *Skin elasticity improvement *Connective tissue tightening *Treatment of pregnancy stretch marks *Treatment of post-liposuction irregularities Applications: *Physiotherapy *Rehabilitation *Sports medicine *Orthopedics *Aesthetic medicine *Treatment for urological pain therapy and erectile dysfunction Demo vedio of the shockwave therapy device https://www.youtube.com/watch?v=xu7Tbmr9dl4 Certificates: CE FDA ISO13485
Work principle: Compressor free ballistic radial shock wave therapy system with electromagnetic generator as projectile accelerator. The hand piece contains a projectile that is accelerated through the electromagnetic transfer of kinetic energy. This kinetic energy is then transformed into impact energy in the applicator head. The impact energy delivered from the applicator head results in radial pulse in the target tissue. Technical specification: Model Number OCE-ESWT-001 Brand name Oceanus / OEM Instrument classification Class II Supply Ability 100 Unit/Units per Month Display Screen 7 inch LCD color touch screen Energy Level 10 to 185 mJ (equivalent to 0.1~5 bar) Operating Frequency 1~22 Hz Operating mode 4 Burst Mode (continuous/4/8/12 shocks) Preset treatment program 7 Preset treatment program Treatment site proposal More than 25 preset treatment recommendations Input voltage 100/240V AC Power Consumption 100/240VAC 50/60 Hz,250VA Fuse wire 250V/10A Service life of handle Minimum 4 million shocks Work enviroment requires 20 ºC -32 ºC 25% -75% RH 700hPa-1060hPa Storage environment requires 0 ºC -40 ºC 10% -93% RH 700hPa-1060hPa Transportation environment requires 10 ºC-70 ºC, 10% -93% RH, 700hPa-1060hPa Feature: *Ergonomic design provides a convenient setting operation *7 inch Display English touch screen design, intuitive *Imported power source, ensuring instant impact output effect *Wide impact pressure and frequency selection , in line with the demand for treatment *Single and dual output options, and offers a variety of specialty probes *7 preset treatment programme , adjustable *Non-invasive completely and no reported side effects, no hospitalization required *No air compressor, portable design and low maintenance cost List of the accessories: Object Quantity Host 1 Therapeutic handle 2 Foot switch 1 Therapeutic head Diameter of 6/15/25mm each 1 Power line 1 Handle pedestal 1 Handwriting pen 1 Silicone cap 10 Aluminum alloy suitcase 1 Product manual 1 Package information: *Dimension: 290*240*130(L/W/H, the host) *Weight: 2.07Kg (the host) *Package method: carton, there is also a aluminum alloy case package inside Warranty: 3 years for the controller unit, 1 year for the accessories. Clinical effect: *Body shapingAnti-cellulite treatment *Scar and wrinkle smoothing *Skin elasticity improvement *Connective tissue tightening *Treatment of pregnancy stretch marks *Treatment of post-liposuction irregularities Applications: *Physiotherapy *Rehabilitation *Sports medicine *Orthopedics *Aesthetic medicine *Treatment for urological pain therapy and erectile dysfunction Demo vedio of the shockwave therapy device: https://www.youtube.COM/watch?V=xu7Tbmr9dl4 Certificates: CE FDA ISO13485
Work principle: The deep muscle stimulator provides deep muscle tissue with kinetic form of percussion and mechanical vibrations, to stimulate proprioceptive functions, relieve muscle pain caused by various conditions like srain, lactic acid build up and scar tissue etc. Technical specification: *Model Number: OCE-DMST-001 *Brand Name: Ocenaus/OEM *Instrument classification: Class II *Supply Ability: 1000 Unit/Units per Month *RPM: 100-3600rpm and adjustable *Power supply: DC24V / 60W, 2.5A / Max, external 100-240V *Frequency: 20-60Hz *Therapeutic head: 12mm/20mm/35mm *Telescopic distance: 6mm *Diameter of the handle: 4.2cm *Treatment depth: 20-40mm *Material of the handle: Stainless steel *Material of the therapeutic head: Titanium alloy Feature: *deep *rapid *short-duration *pain relief List of the accessories: Object Quantity Handle 1 Therapeutic head 12mm/20mm/35mm each 1 Power line 1 Power adapter cable 1 lubricating oil 1 Package information: *Dimension: 240*50*136mm (L/W/H, the handle) *Weight: 2.5KG (the handle) *Package method: carton, there is also a aluminum alloy case package inside Warranty: 1 year for the controller unit and the accessories. Clinical effect: *complete pain relief, quick repair the injured tissue *increase the rate of blood flow *increase lymph flow *reduce post-surgical swelling and pain *reduce muscle spasm *reduce muscle soreness *reduce pain in oversue injuries of the knee *improve relaxation *release adhesion *break down calcification *dilate blood vessels *promote metabolism *reduce lactic acid build up *Use DMS before and after exercise can ease muscle pain Applications: *Effective managment of acute & chronic pain *Musculoskeletal Dysfunction *General or localized muscle spasm *Soft tissue injuires including sprain, strain *Integrated Manual Therapy *Treat Connective tissue Certificates: CE FDA ISO13485
Product Description : probe material: medical ABS metal electrodes: stainless steel probe total length: 10.4cm probe available length: 9cm probe maximum width: 3.4cm PVC line length: 23mm The merits: has a unique rectangular section that resists lateral movement An External flange to assist retention Softly curving form assists insertion and comfort in use The contoured electrodes provide comfortable stimulus Its narrow neck allows surrounding tissue to take on its natural form Soft, flexible leads provide remote and hygienic connection to equipment weight: 60g
Features: True lcd display Light weight, easy for use Fhr waveform and numeric display;optional temp probe Low ultrasound level, safe to fetus Specifications: Working frequency: 2.5mhz Working mode: pulsed doppler Ultrasound strength: < 5mw/cm2 Unit dimension:3.2*9.6*13.8cm Unit weight: 170g with battery Moq: 25pcs/carton Carton size:0.53(l) *0.43(w)*0.41(h) Carton volume weight: 19kg
