Features:
Stage ll medium treatment APP overlay
A-B line air tubes alternating for pressure relief,anti bedsore/decubitus
Top grade TPU from Taiwan
Double CPR,Pillow function,Ventilation,Cover with zipper closure.
Warranty:12months
Â
Â
APP-P08B Air Pump
Features:
Aluminum motor cover,good heat dissipation, anti=vibration.
Knob control panel,easy to operate
Ultra silence, noise 20<=dB
Warranty: 2 years
Specifications:
| Pump | Pad |
| Item: APP-P08B | Item: APP-T03 |
| Power supply: 110V/60Hz or 220V/50Hz | Size: 80inch L*32-36inch W*4inch H (24 cells) Â Â Â Â Â 4.5"Â 18Â cells and 5" 16 cells for more options |
| Air output:7-8 L/min. | Mattress material: Nylon /TPU |
| Pressure range: 25 mmHg - 140 mmHg | Cover material: Nylon PU |
| Cycle time: 12 min. | Bottom material: tarpaulin PVC |
| Power consumption: 7W | Mattress weight :4.48kgs |
| Fuse: 1A | Weight Capacity: 150kg |
| Size: 27cm(L) x 13cm(W) x9cm(H) | Â |
| Weight:1.29kgs | Â |
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RT-PCR Test Reagent Kit Of COVID-19(ORF1ab, N)
The RT-PCR Test Reagent Kit Of COVID-19(ORF1ab, N) is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate) from individuals suspected of COVID-19 by their healthcare provider.
Results are for the identification of SARS-CoV-2 RNA.The SARS-CoV-2 RNA is generally detectable in upper and lower respiratory specimens during the acute phase of infection.
Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infective status. The agent detected may not be the definite cause of disease. Positive results do not rule out bacterial co-infection with other viruses.
Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information. The COVID-19 RT-PCR Detection Kit is intended for use by qualified trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures.
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Shenzhen Uni-medica Technology Co.,Ltd , https://www.nbunimed-global.com