Poc quantitative reader for rapid test, animal disease diagnosis test uncut sheet.
Genbody Poc test kit available in quantity. we carry home kit as well flowFlex iHealith and more.
Spesification Red Colour Semi Organic use POC organic have cerificate from surveyour goverment of indonesia
Walnut kernel, flaxseeds, pumpkin seeds and kernels, sunflower, seed and sunflower seed kernels.
Flax seeds, walnuts inshell, walnuts kernel, pumpkin seed, pumpkin seed without shell, sunflower seed without shell.
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Pumpkin seeds, sunflower seed kernels, linseeds, walnut.Producer
Access Bio CareStart rapid antigen POC test kits - We are now shipping (within the US) by the pallet at as low as $10.00 per test. 20 pcs per kit/box, 640 boxes per pallet.
Celltrion Diatrust covid-19 Ag rapid tests We have the ability to supply both POC as well as OTC kits. POC kits start at $4.25 per test. OTC kits start at $6.75 per test. All Test Kits are OTG in the US at the Celltrion Warehouse. Delivery is available for a minimal fee, or no fee at all depending on the order. The Test Kits are either picked up at the Celltrion warehouse in TN or NJ or drop shipped to your facility. For large Bulk orders with weekly or monthly allocation, a 10% deposit is required to reserve the specific allocation, and the balance is paid prior to pickup or delivery. Both the POC and OTC Test Kits are available for delivery also in large quantities, however due to the high demand, a pick up schedule or delivery schedule will be determined at the moment the PO is issued and will become an integral part of the supply agreement.
Printers off-cuts waste (poc) Coated book stock (cbs) Sorted office paper (sop) Old corrugated cardboard (occ) Mixed waste paper (mix) Magazine sections (glue free) Fly leaf shavings (glue free) Poly coated milk carton (pcmc) Sorted white ledger (swl) Soft white Newsprint (onp) 1 bale = 1x1m3 Weigth 1 bale = 500kg
Quidel Droppers Clear Quidel has manufactured the QuickVue line of products for hospital and physician office labs for over 30 years. QuickVue rapid lateral flow tests produce accurate results in minutes, allowing for faster diagnosis and treatment. QuickVue products encompass areas of infectious disease, women's health and general health. These tests include Influenza, RSV, Strep A, fecal occult blood, pregnancy, chlamydia, infectious mononucleosis, and H. pylori. QuickVue products have continued to deliver quality results with a variety of formats well suited for both POC and laboratory needs.
Peltier-type & whisper-quiet Mini Dehumidifier with POC & ionizer, energy saver choice to dehumidify and purify the air in small area, such as bathroom,laundry room, or closet etc. -Dehumidifying capacity at 30°C 80% RH -Dehumidifier with 500ml water tank -Automatically switch off when the tank is full (With LED indication) -AC/DC adaptor available -Modern design with warm air outlet for drying -Compressor free -Low power consumption -For small areas use,such as bedroom,bathroom,storage,garage,nursery, dormitory,car,boat and mobile container -PCO & lonizer(optional) -Dimension: 140X120X200mm
OCC#11, NCC, SKC, FC, HWS, SWL, POC(PSOP), POC(SOP2), BBC, PBBC, NEWS(ONP), cup stocks, soft mixed paper, hard mixed paper.
The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within the first five days of symptom onset or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet the requirements to perform moderate, high, or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., inpatient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation. Lateral flow assay Detect SARS-CoV-2 nucleocapsid protein antigen Rapid results within 10-15 minutes Intended at POC setting (i.e., in patient care settings) by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation For use under the Emergency Use Authorization (EUA) only For in vitro diagnostic use only For prescription use only For use with direct anterior nasal and nasopharyngeal swab specimens Clinical Performance 93.75% PPAa and 99.32% NPAb when used with nasopharyngeal swab 87.18% PPAa and 100% NPAb when used with anterior nasal swab
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X Ray Films, Paper (POC), Carton (OCC and NCC), Polycarbonate bottles (PC), Over Isued Newspaper (OINP).
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CLIA Waived Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests. This test is also authorized for use with fingerstick whole blood specimens only at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation. The COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only. Indication: Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. About Test Device EUA Authorized Gives Positive or Negative Result for COVID-19 virus Read Results in 15 Minutes 24 Month Expiration from Date of Manufacture Contents 20 Test Devices 20 Disposable Pipettes 20 Alcohol Prep Pads Sterile Safety Lancets Buffer Package Insert
CLIA Waived Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests. This test is also authorized for use with fingerstick whole blood specimens only at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation. The CLIA Waived COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only. Indication: Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized laboratories. About Test Device EUA Authorized CE Mark Test does NOT give positive or negative result for COVID-19 virus. This is an antibody test, it only indicates past or recent infection. Read Results in 15 Minutes 9 Month Expiration from Date of Manufacture Contents 20 Test Devices 20 Disposable Pipettes 20 Alcohol Prep Pads Sterile Safety Lancets Buffer Package Insert
Approach to¡ê¡§near¡ê© perfect eye diagram index Each repeater with power and sdi format indicate, user can real-time monitor conveniently Built-in esd protection circuit to avoid electrostatic damage effectively Mini appearance, easily to setup and use Special features Supply the power from sdi monitor room (dvr side) through coax with poc technology to front repeater 1 channel reverse 5m wide band data channel with doc technology be debug Ed to vedio cable, the front camera can be controlled by control signal(rs485) through coax in monitor room. 2/4/8ch sd/hd/3g-sdi repeater is applied for extending sdi signal transmission. It can be distribute the sdi to 2/4/8 way and very easily to save the setup space, simplify the power supply, easily to setup and maintenance and save the cost through single equipment connect with 2/4/8 way sdi signal. 2/4/8ch sd/hd/3g-sdi repeater which with equalizer of circuit, re-clocker, and cable driver, can recover the signal attenuation though long distance, can be distributed various channel and long distance driver extending, which has perfect eye diagram index when use tektronix/phabrix etc. Professional instrument to detect. 2/4/8ch sd/hd/3g-sdi repeater support all sdi format smpte-424m 3g-sdi, smpte-292m(hd-sdi), smpte-259m sd-sdi component signal video and dvb-asi signal, which coincidence ¡ê¡§comply with ¡ê©smpte standard and meet the requirement of broadcast signal transmission. (coincidence the transmission level of broadcast grade.) Outer carton dimension ¡êo26*24*8 cm Weight: 1.5kg Packing: package by carton
