首暉國際有限公司

Square Type Emergency Light

Escape & Emergency Luminaire （ESA09）

Escape & Emergency Luminaire （ESA08）

Escape & Emergency Luminaire (ESA05)

LED Emergency Down Light

Escape & Emergency Luminaire

Led Emergency Down Light

Round Type Emergency Light

LED Emergency Bulk Head (BK2)

Emergency Bulk Head / Exit Sign

朗怡國際有限公司

Covid-19 Rapid Test Kit comply with ISO 13485:2016
Fast detection of COVID-19 	 The test can be performed in 10 minutes from patients&#39; whole blood,&nbsp;serum or plasma.  Suitable for testing a large number of patients 	 Due to its simplicity and minimal sample preparation time, this kit&nbsp;can be used in a wide range of settings (clinics, transport hubs,&nbsp;schools).  Ability to estimate the time of infection 	 Based on the immunological profile (IgG/IgM ratio) the stage of&nbsp;infection can be predicted.  Affordable testing expenses 	 Since highly trained personnel or expensive equipment is not needed,&nbsp;the cost of testing is relatively low. 	 MOQ will be 20 pcs in a box package.  

Covid-19 Rapid Test Kit Comply 

MGM Industries & Company

The iHealth® COVID-19 Antigen Rapid Test is a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2.  This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older with symptoms of COVID-19 within the first 7 days of symptom onset. This test is also authorized for non-prescription home use with adult-collected nasal swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first 7 days of symptom onset.  This test is also authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older, or adult collected anterior nasal swab samples from individuals aged 2 years or older, with or without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests.  This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA; This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and, The emergency use of this product 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 Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.  Disclaimer: If you’re currently experiencing COVID-19 symptoms, please contact your primary care physician (PCP) for immediate guidance. iHealth® COVID-19 Antigen Rapid Test may take several days to ship. This is not a PCR test and not valid for travel. The manufacturer of the iHealth® COVID-19 Antigen Rapid Test requires test kits be stored at temperatures between 36o and 86oF (2o - 30oC). Any extended exposure of the test kit to temperatures beyond this range may affect quality of test results. If you have ordered home delivery of the test kit and expect temperatures in your area to be outside of this range at time of delivery, it is recommended that you arrange for someone to be home at or near time of delivery to receive the test kit. 

 COVID-19 Antigen Rapid Test Self-Test at Home

新空實業有限公司

iPhone 5S Extension Testing Flex Cable for LCD spare parts, 1. Fully replacement and fit for iPhone 5S models. 2. Brand new condition. 3. Good quality for refurb market.    

iPhone 5S Extension Testing Flex Cable for LCD

東美實業有限公司

 COVID-19 IgG/IgM Rapid Test &amp; SARS-CoV-2 Proteins 

Serological immunoassay is an important auxiliary method for the diagnosis of COVID-19. The combination with molecular diagnostic is helpful to improve the accuracy of COVID-19 detection.&nbsp;
-&nbsp;Result available in 10-15 minutes.
- Whole blood, serum and Easy storage, 4-30&deg;C.

The colloidal gold immunoassay (CGIA) to detect COVID-19 utilizes the specific reaction between anti gen and antibody to detect the anti-SARS-CoV-2 antibody in patients&#39; sample. The advantages of CGIA is fast and convenient, stable sample collection, high throughput, and the result can be interpreted by naked eye.

 Product Features: 
COVID-19 IgM: 167 clinical specimens from individuals suspected of COVID-19 infection were detected by COVID-19 IgG/IgM rapid test cassette of CLONGENE&reg;, The result was compared with that of RT-PCR.

 Reproducibility: 
0 clinical serum specimens include 20 negative, 20 borderline positive and 20 posi- tive were tested in three physician office laboratories (POL), and each specimen was tested for three days at each POL. The intra-assay agreements and the in- ter-site agreement was both 100%.

 Specificity: 
- No cross reactivity was observed with specimens from patients infected with HIV, HAV, HBSAG, HCV, TP, HTLV, CMV, FLUA, FLUB, RSV, MP, CP, HPIVs.
-&nbsp;Common serum components, such as albumin, bilirubin, hemoglobin, et. al., do not Interfere with the COVID-19 IgG/IgM rapid test cassette of CLONGENEⓇ
- No cross reactivity or interference was observed with common biological analytes.

COVID-19 Rapid Test

Introduction: This equipment provide a long time stable environment of temperature, humidity and illumination for the Pharmaceutical industry medicine invalidation evaluation. It’s applied in the medicine accelerating test, growth test, high humidity test and high illuminance test. Features: *The Inner chamber is 304 high-quality stainless steel, full arc design, easy to clean and maintain. *The unique air duct design ensures the uniform temperature and humidity in the box. *Remote monitoring via mobile phones and computers. *It has three levels of password authority management function. *Data recording system can record more than 1 million pieces of data, even if the power failure, the data will not be lost,  can be exported through the U disk. *Conforms to the national pharmacopoeia, GMP, FDA, ICH and other relevant standards for long-term test, intermediate  test, accelerated test, with stable and reliable performance to meet the requirements of temperature, humidity, light and  other environmental conditions in multiple drug tests.   

Medicine Stability Test Chamber

Application Range: This equipment provides a long-time stable environment of temperature, humidity and illumination for the pharmaceutical industry medicine invalidation evaluation. It’s applied in the medicine accelerating test, growth test, high humidity test and high illuminance test.  Features: *P.I.D accurate and reliable temperature and humidity control. *Built-in fan to form air circulation and improve temperature uniformity inside the cabinet. *Built-in water tank and automatic water replenishment interface, when there is no humidification water, automatically disconnect the heater power. *50 pcs programs for the pharmaceuticals application. *600-day historical data USB export function. *Optional : Printer, External temperature protection device.    

Application: BK-TS200 lab test sieve is suitable for particles distribution analysis. It is primarily used to determine particle size distribution for particles, powder and liquid in laboratory and quality control department.  Features: * Screen mesh size range: from 4 mesh to 500 mesh. * Timing range: 0-99 min 59s, time can be set from seconds to hours freely. * Typically requires 50-150g of sample material.   

Laboratory Test Sieve

Application Range: This equipment provides a long time stable environment of temperature, humidity and illumination for the pharmaceutical industry medicine invalidation for the pharmaceutical industry medicine invalidation evaluation. It’s applied in the medicine accelerating test, high humidity test and high illuminance test.  Features: * P.I.D accurate and reliable temperature and humidity control. * Built-in fan to form air circulation and improve temperature uniformity inside the cabinet. * Built-in water tank and automatic water replenishment interface, when there is no humidification water, automatically disconnect the heater power. * 50 pre-set programs for the pharmaceuticals application. * Standard Accessory include: USB port. * Optical : Printer, External temperature protection device.   

 COVID-19 Antigen Rapid Test Cassette (Swab) 
Designed for qualitative detection of SARS-CoV-2 antigen in Swabs

 SARS-CoV-2 Nucleocapsid Protein Detection 
Nucleocapsid [N] protein is the most abundant protein with highly conserved in SARS Cov 2. N protein is used as the core raw material of rapid diagnostic reagent for immunalogy in the market.

 COVID-19 Antigen Rapid Test Cassette 
We has developed the COVID-19 Antigen Rapid Test Cassette. The colloidal gald immunoassay (CGIA) to detect nucleacapsid protein of SARS-CoV-2 is based on the principle of the double antibody -sandwich technique.

The combination of COVID-19 Antigen Rapid Test and COVID-19 IgG/IgM Rapid Test can improve the accuracy of SARS-CoV-2 (COVID-19) detection. We also can provide the COVID-19 IgG/IgM Rapid Test Cassette. Please contact us for more information.

COVID-19 Antigen Rapid Test Cassette (Swab)

紹興上虞明吉塑業有限公司

INJECTION-MOLDED THERMOPLASTIC ABS HOUSING, SUITABLE FOR WALL MOUNT, 120V/277V DUAL VOLTAGE OPERATION, BUILT-IN 3.6V 700MHA BATTERY, MINI 90 MINUTES IN EMERGENCY MODE, TEST SWITCH AND CHARGE INDICATOR, UL AND CUL LISTED. 

LED EMERGENCY EXIT LIGHT 

SMD 2*1.2W led heads, 24pcs SMD Leds,120-277V universal voltage, LED indicator, Push button test switch, 3.6V 700mAH Ni-cd battery, More than 90mins on emergency mode, UL approved 

Easy-to-use nasal swab test Requires just 1 test* Can be used to test children as young as 2 years old For use with and without COVID-19 symptoms Accurate results in 15 minutes No need to send off to a lab to obtain results Compact packaging for “On-The-Go” testing *Other COVID-19 antigen home tests may require a 2nd test 2-3 days after the first.  This product has not been FDA cleared or approved but has been authorized by FDA under an EUA.  This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens.  The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated, or authorization is revoked sooner. 

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