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Top Supplier Cities : Shenzhen   -   Shanghai  
Feb-16-22
 
Rapid Antigen Test Card
Self-test received notified body approved CE marking on Apr.1,2021

A home test for the rapid qualitative detection of antigen in anterior nasal swabs within 7days of symptom onset
â?¢Sample type: nasal swab
â?¢Time to result: 15-20 min
â?¢Sensitivity: 96.77%Specificity: 99.20%Accuracy: 98.72%
â?¢Layperson study statistics:
99.10% of non-professionals carried out the test without requiring
97.87% of different types of results were interpreted correctly
Each Test have Unique Identifier Number - Easy to track
Approved By - UK, Germany, France, Spain, Netherlands, Greece, Belgium, Italy, Portugal.

1 Test / Kit
Catalog No.: 1N40C5-2
Kit Components:
1 Rapid SARS-CoV-2
Antigen Test Card (sealed
foil pouch)
1 sterilized swab
1 extraction tube
1 sample extraction buffer
IFU
Tube holder on back of box

Box / Carton Specifications :
1 Test / Kit
Box size - 190*60*15 mm
Carton size - 42*42*33 cm
250 tests (boxes) / carton
Carton gross weight - 9.9 kg


Price and Minumum Quantity
Price FOB in USD: -Minimum Order Qty: 2000 Pieces
Production Capacity: 10 Million Units A MonthPackaging: Pack Of 1, 5, 20
Product Model And Origin: Xiamen China
Brand: BOSON
Sep-01-10
 
Rapid Influenza A + B Test Card

Intended Use
Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture.

Contents of Kit
Flu A + B Test Card 20 ea
Sample Extraction Buffer 1 ea
Extraction Tube 20 ea
Nozzle With Filter 21 ea
Sterilized Swab 20 ea
Tube Stand 1 ea
Instructions For Use 1 ea

Storage And Stability
Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial.

Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after the expiration date.
3. The test device should remain in the sealed pouch until use.
4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test.
5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers.
6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation.
7. Visibly bloody samples should not be used for the testing.

25 tests/kit, 40 kits/carton
Nov-05-14
Supplier From Xiamen, Fujian, China
Jan-27-21
Supplier From Xiamen, Fujian, China
Mar-22-22
Supplier From Xiamen, Fujian, China
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Feb-03-21
Supplier From Xiamen, Fujian, China
Jul-22-21
Supplier From Xiamen, Fujian, China
Nov-16-20
Supplier From Xiamen, Fujian, China
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