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Faraz

Supplier From Pakistan
May-28-20
Supplier : A new product for COVID 19

Established: 2020

Verification Status



Contact Details:
Home Town Yaseen,province Giligit Baltistan.country Pakistan
Ghizer O92
Gigil Pakistan


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May-02-20
Supplier From Amsterdam, Singapore
 
* NEW* Covid-19 ANTIGEN RAPID TEST KIT *NEW * with CE Mark EU APPROVED | Collodial Gold Method | 15 Minutes Rapid

Covid-19 Rapid Antigen Test Kit | Collodial Gold Method
Accurate: 96.1% sensitivity, 96.67% specificity compared with PCR
FAST: only 15 minutes required
EASY-TO-USE: no special requirements
Room temperature storage
MOQ 2000 units (25pcs) per unit
MAX 300.000 units PER DAY

Payment terms
100% TT in Advance
Lead time 7 days
Global delivery
Results
May-20-20
 
Name:Temperature measuring Bracelet
Design:Bar
Movement Type:Electronic
Band Material:TPU
Case Material:ABS
Function:24 hour instruction, Alarm Clock, Countdown, Call Reminder, Fitness Tracker, Heart Rate Tracker, MONTH, Message Reminder, Push Message, Sleep Tracker, WORLD TIME, chronograph, THERMOMETER
Resolution:80*160
Touch mothed:Single point
Bluetooth version:4.0
Special Function:Body temperature measurement
Battery:90mAh
Charging Method:Built-in USB
Waterproof:IP68
UI Languages:English, Chinese
Compatible:Android 4.4/ios8 or above
Apr-13-20

Covid-19 New Coronavirus Test Kit

$1.00
MOQ: Not Specified
Supplier From London, Bedford, United Kingdom
 
Contraindications, precautions, warnings, and instructions:
Found that the original packaging is damaged and prohibited to use.
Sterilized with ethylene oxide.
Contact Directly
This products is limited to one-time use and is it destroyed after use.
Prohibited to use after the expiration date.
Dec-30-20
Supplier From Shenzhen, Guangdong, China
 
Intended use:
AIVD COVID-19(SARS-CoV-2) IgG/IgM Rapid Test is a single use, rapid device for qualitative detection of total antibodies against 2019 novel coronavirus (SARS-CoV-2) in human serum, plasma or whole blood specimens. The kit is intended for screening of patients suspected for infection with SARS-CoV-2, and as an aid in the diagnosis of the coronavirus disease 2019 (COVID-19).

Descriptionï¼?
Novel coronavirus pneumonia (NCP) or SARS-COV-2, that was officially named by the WHO as â??Corona virus disease 2019â?? (COVID-19), is a respiratory infection caused by a new virus that was first identified in late 2019.

IgM/IgG Rapid Kit can specifically detect IgM and IgG antibodies of COVID-19, covering the entire course of infection and recovery period of patients. This approach improves the overall diagnosis of COVID-19 in both acute and recovery phases of illness.

This kit utilizes the principle of colloidal gold immunochromatography to qualitatively detect the new coronavirus (COVID-19) IgG / IgM antibodies in human serum and plasma. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of COVID-19 suspected patients.

This method does not require expensive medical instruments and consumables. Just take the specimen and add it to the sample well, and then add the required amount of a diluent. The IgG / IgM antibodies in the sample will interact with the colloidal gold-labeled COVID-19 recombinant antigen on the conjugate pad. Then the conjugate pad will release re-solubilized conjugate onto the nitrocellulose membrane. The nitrocellulose membrane (NC membrane) diffuses it forward.
As the sample moves along the device binding reagents situated on the nitrocellulose membrane bind to the target at the test line. If the sample contains a COVID-19 IgG antibodies, they will bind to the colloidal gold-labeled novel coronavirus recombinant antigen, diffuse forward, and then react with the anti-human IgG antibodies immobilized on the NC membrane detection line (T2 line). Similarly, if the specimen contains IgM antibodies to COVID-19, the antibodies will react with antigen-coated particles, the conjugate migrate laterally forward, and cause a colored line (T1 line). The darker the color of colloidal gold on the test line, the higher the concentration antibodies to COVID-19 in the sample.

Accuracy:ï¼?> 90%
Specificity: 97%


Basic Protocolï¼?
1. Remove the test specimen, required reagents from storage conditions, and equilibrate to room temperature.
2. Unpack the aluminum foil bag, place the test horizontally on the table and number it.
3. Add 10ul serum, plasma or whole blood sample to the sample well with a pipette or a dropper. Slowly add 2 drops of sample dilution (about 60uL) to the sample well.
4. Read the results within 10-15 minutes after adding the sample, and the results will be invalid after 30 minutes.
Dec-30-20
Supplier From Shenzhen, Guangdong, China
 
AIVD Biotechs COVID-19 Ag test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein (NP) antigen from SARS-CoV-2 in direct nasal swabs from individuals suspected of COVID-19.

Description
This kit utilizes the principle of latex bead immunochromatography to qualitatively detect the new coronavirus (COVID-19) Np antigen in human nasal swabs. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of COVID-19 suspected patients.
The test contains latex bead conjugate pad and a membrane strip pre-coated with antibodies specific to SARS-CoV-2 antigen on the test lines (T). If SARS-CoV-2 antigen is present in the specimen, a visible band appears on the test lines (T) as antibody-antigen-antibody latex bead complex forms. The control line (C) is used for procedural control and should always appear if the test is performed correctly.
This method does not require expensive medical instruments and consumables. Just take the specimen and add it to the sample well. If sample contains the antigen, it will interact with the latex bead-labeled COVID-19 anti-SARS-COV-2 NP antibodies on the conjugate pad.

Required components
1. A foil pouch with a desiccant and a single-use test card, 1 piece
3. Sterile swab, 1 piece
3. Extraction buffer tube (1 ml), 1 tube.
4. Instructions for use, 1 piece.

Specimen requirements:
1. Nasopharyngeal swab specimen.
2.Specimen should be tested as soon as possible upon collection. If the sample has to be stored, store the swab sample at room temperature for up to 1 hour or 2~8â?? for up to 4 hours prior to testing.

Specimen preparation
1. Insert the extraction buffer tube into the tube rack, make sure that the sample tube is firmly upright and touches the bottom of the rack.
2. Insert the swab into an extraction buffer tube.
3. Gently stir the swab in the tube, and then left swab inside the tube for 1 minute or Mix on the vortex mixer for about 30 seconds,
4. The sample should be tested immediately after collection.
If it cannot be tested in time, it should be stored in the virus transport matrix. The specimens can be stored at 2-8C for 4 hours

Basic Protocol
Step 1: If the sample is refrigerated, remove the sample to be tested and the required reagents from the storage conditions, equilibrate to room temperature (15~30C)
Step 2: When preparing to test, open the aluminum foil bag, take out the test card, and lay it flat on a table.
Step 3: Mark the sample number on the test card,
Step 4: Using pipette add 50ul of the sample into a sample well on the device,
Step 5: Read the result within 15 minutes,
Please read the result after 15 minutes. After observing and recording the result, please discard the test card to avoid affecting the result judgment.
Do not read test results after 30 minutes. It may give false results.
Feb-09-21
Supplier From Pune, Maharashtra, India
 
Antigen Rapid COVID 19 Test

Simple nasal swab or nasopharyngeal swab
under 30 minutes
Sensitivity 97.10%
TCID50 75.5
CE marked for diagnostic use in EU and associated countries
Paul Ehrlich Institute and IVD
Min order 10000 pcs
Free delivery within Germany
Dec-30-20

Covid-19 Test Kit

$2.31
MOQ: Not Specified
Supplier From Incheon, South Korea (Republic Of Korea)
 
We, CentZone, are proudly offer you COVID-19 Self-Test Kit as below.
Required document must be submitted in order to provide detail information of each Test Kits.
Otherwise no information will be available.

If you are willing to order and purchase below COVID-19 Self-Test Kits, please do send below information in LOI contract by return at oversea@centzone.co.kr

[Required Documents]
* LOI Contract
- LOI contract must include below information as a mandatory
- Local sales company information including Tel, Address, E-mail, Website, Business Registration Number and name of the person in charge.
- Company Profile for both broker and end-sales company.
- Yearly Forecast Volume

[COVID-19 SELF-TEST KIT PRODUCT]

1. Genbody COVID-19 Self-Check Kit
*FDA Certificates.
(1) Professional Use : MOQ 100,000 Kits
$5.00/Kit --> 25 Kits per Set
(2) Home Use : MOQ 100,000 Kits
$6.00/Kit --> 2 Kits per Set

2. Celltrion COVID-19 Self-Check Kit
*FDA Certiticates.
(1) Home Use : MOQ : 100,000 Kits
$8.00/Kit --> 2 Kits per Set

3. G-Mate(Filosys) Saliva COVID-19 Self-Test Kit
* Accuracy : +98%
* MOQ : 1,000,000 Kits
(1) $3.0 / Kit : 25 test kits per box
(2) $3.2 / kit : 1 test kit per box

4. ND Force Saliva COVID-19 Self-Test Kit
* Accuracy : ±94%
* Recently approved by German FDA.
* CFS(Certificates of Free Sales) can be provided direcctly from German FDA.
* 1 Kit per Set.
- MOQ 100,000 Kits : U$2.60
- MOQ: 500,000 Kits : U$2.50
- MOQ: 1,000,000 Kits : U$2.30

Look forward to your PO.

Sincerely,

Andrew. Kim
CentZone Oversea Sales
May-27-20

Covid 19 Detection Kit

$17.00
MOQ: Not Specified
Supplier From Daejeon, Daejeon, South Korea (Republic Of Korea)
 
Unit Price: USD 17

Target Region: ORF1ab, N gene

Accuracy: 100%

Recommended PCR:
CFX96 Real Time PCR System (Bio Rad)
ABI7500 Real Time PCR System (Thermo Fisher Scientific)

Box Size: 10 cm * 6.5 cm

Certification:
ISO 13485
ISO 9001
Korea GMP
European CE
USA EUA
Jun-28-20

Covid-19 Diagnostic Kit

$1.00
MOQ: Not Specified
Supplier From Busan, South Korea (Republic Of Korea)
 
Covid-19 Diagnostic Kit(Made in Korea)

PCR running Time : 30m
May-04-20

Covid 19 Test Kit

$1.8k
MOQ: Not Specified
Supplier From Incheon, South Korea (Republic Of Korea)
 
We are supplying FDA's EUA approved Covid 19 Test Kit to the US.

Our COVID-19 Detection Kit is a real-time PCR based in-vitro diagnostic product intended for detection of the novel coronavirus
SARS-CoV-2 (COVID-19) RNA in sputum, bronchoalveolar lavage, oropharyngeal or nasopharyngeal smears collected from patients with
suspect viral infection
The kit is composed of Internal Positive Control (IPC), to monitor appropriate performance of amplification and detection of the kit.
Accurate detection of the viral RNA is confirmed parallelly by using Positive and Negative controls which are composed in the kit

Verification Status