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Place of Origin:CHINA Material:Stainless Steel Application:Construction Machinery Color:Sliver Warranty:1 Year MOQ:1 Pieces Type:Fittings Packaging & Delivery Selling Units:Single item Single package size: 20X8X8 cm Single gross weight:0.500 kg Package Type:normally packing
Face shield PRICE/PC CIF Major ports worldwide USD1.10/pc It consists of a protective cover, foam strip and fixing device made of polymer materials. 2. Nonsterile, single-use. 3. Anti-fog CE/FDA certificates 200/CTN 67.5X44X36 CM 0.1 CBM/CTN 600 ctns, 120,000 pcs / 40'HQ container 280 ctns 56000 pcs in 1x20 container
nitrile gloves Nitrile Gloves,3-Mil,Large,Powder-free,Latex-free,Non-medical FOB Shanghai USD0.08/pc USD0.10/pc CIF destination port CE/FDA certificates 1 20' container holds 1400000 1.4 million gloves, delivery 1-2 weeks. 40' container holds 3400000 3.4 million
PRICE/PC CIF Major ports worldwide USD0.11/pc 3ply face mask, civil protection 50pcs/box*40 box (2000 pcs) per carton 18*10*8cm/box 52*38*34cm/ctn 0.0672 cbm/ctn 970 CTNS 1,940,000 PCS Production capacity 30,000,000pcs/month
PRICE/PC CIF Major ports worldwide USD1.35/pc Protective Coverall and Gowns (PPE)- Size Medium (Level 2), PP+PE laminated protection gown, ultrasonic, long sleeves with neck and waist tie CE/FDA certificates 10pcs/bag, 100pcs/carton 50*28*42 50*28*42. 0.061 cbm/ctn 1x40â??HQ container 1120 ctns 112000 pcs 1x20â?? container 470 ctns 47000 pcs
Sample Types : Including Nasopharyngeal swab, Oropharyngeal swab, Sputum Controls : Internal control, UNG enzyme and dUTP used to reduce risk of contamination, false positive and false negative results Product Information 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. Authorized Laboratories Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. About Emergency Use Authorization (EUA) This test (1) has not been FDA cleared or approved, (2) has been authorized by FDA under an EUA for use by authorized laboratories, (3) has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens, and (4) is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C.360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
The COVID-19 RT-PCR Detection Kit 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. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C. 263a, to perform high complexity tests. 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. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities. 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. The COVID-19 RT-PCR Detection Kit is only for use under the Food and Drug Administration's Emergency Use Authorization. PRINCIPLE OF DETECTION This product is a fluorescent probe-based Taqman RT-PCR assay system. Firstly, the RNA of SARS-CoV-2 will be reverse transcribed into cDNA by reverse transcriptase, and then PCR amplification will be performed with cDNA as template. During amplification of the template, the TaqMan probe will be degraded due to the 5'-3 polymerase activity and exonuclease activity of Taq DNA polymerase, then the separation of fluorescent reporter and quencher enables the fluorescent signal to be detected by instrument. The ORF1ab gene of SARS-CoV-2 will be detected qualitatively by FAM channel, the N gene of SARS-CoV-2 will be detected qualitatively by JOE channel, the E gene of SARS-CoV-2 will be detected qualitatively by ROX channel, and the internal reference will be detected by CY5 channel. dUTP and UNG enzyme are used in the kit to prevent contamination of the amplified products. Internal reference is used in the kit for quality control starting from sample collection
Indication: Qualitative detection of nucleic acid from 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. Emergency use of this test is limited to authorized laboratories. Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. This letter is in response to your1 request that the Food and Drug Administration (FDA) issue an Emergency Use Authorization (EUA) for emergency use of your product,2 pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. 360bbb-3). On February 4, 2020, pursuant to Section 564(b)(1)(C) of the Act, the Secretary of the Department of Health and Human Services (HHS) determined that there is a public health emergency that has a significant potential to affect national security or the health and security of United States citizens living abroad, and that involves the virus that causes COVID-19. Pursuant to Section 564 of the Act, and on the basis of such determination, the Secretary of HHS then declared that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of the virus that causes COVID-19 subject to the terms of any authorization issued under Section 564(a) of the Act. Having concluded that the criteria for issuance of this authorization under Section 564(c) of the Act are met, I am authorizing the emergency use of your product, described in the Scope of Authorization of this letter (Section II), subject to the terms of this authorization. I. Criteria for Issuance of Authorization I have concluded that the emergency use of your product meets the criteria for issuance of an authorization under Section 564(c) of the Act, because I have concluded that: 1. The SARS-CoV-2 can cause a serious or life-threatening disease or condition, including severe respiratory illness, to humans infected by this virus; 2. Based on the totality of scientific evidence available to FDA, it is reasonable to believe that your product may be effective in diagnosing COVID-19, and that the known and potential benefits of your product when used for diagnosing COVID-19, outweigh the known and potential risks of your product; and, 3. There is no adequate, approved, and available alternative to the emergency use of your product. 4 II. Scope of Authorization I have concluded, pursuant to Section 564(d)(1) of the Act, that the scope of this authorization is limited to the indication above.
Commodity: Covid-19 RT-PCR Detection Kit Spec.96 tests/kit Price:FOB SHANGHAI USD3.30/test, USD316.8/kit $3.60/TEST CIF NY AIRPORT OR OTHER MAJOR AIRPORTS USA OR EUROPE OR S. AMERICA OR MIDDLE EAST Payment: T/T ADVANCE 50% BALANCE BEFORE DEPARTURE OR Sight Irrevocable TRANSFERABLE LC Delivery: By AIR, 50days after receipt and confirmation of LC
Ppe items, mask, face shield, isolation gowns, gloves, and covid test kits, toys, electronics, cell phones, hardware, pp raw material or polypropylene.
PPE, hand sanitizer, wooden tray, plywood, wooden pallet.
Glass paper weights Wc and supply many size and designs of hand made glass paperweights. 20 oz
Face mask medical coverall.Business consulting, business opportunities introduction, business background dd
Lithium battery pack 12V 200Ah Capcity 2,560Wh Nominal voltage 12.8V Nominal capacity 200Ah with BMS, 0.5C LiFePO4 lithium battery cell 3.2V 2,000 deep cycle life Application in marine and solar
3 Ply Surgical Face Masks Specifications: Type IIR 50 Pcs. Per Box 3 Layers Various Colors BFE >98%
Product structure: Three layer non-woven fabric, double layer melt blown fabric Specification model: 16cm*10.5cm Application : This product is suitable for daily protection of polluted air, haze weather and dusty environment.
We have 100,000 pieces N95 masks in stock in Los Angeles,NIOSH approved and FDA certification 510k K122702,please feel free to contact me!thank you .
Mask, Goggles, Latex Gloves, Infrared Thermometer and Protective Clothing.ODM & OEM Service, Trades Distributors, designing and manufacturing
