Supplier : Fertility hormone for hcg, lh, fsh;infectious diseases & std for hbsag, anti-hbsab, hcv, hiv 1/2, hiv saliva, syphilis, malaria, dengue, h.Pylori, tb, chlamydia, conorrhea, typhoid, rotavirus, adenovirus, tumor markers for afp, cea, psa, fob;drug of abuse for amp, coc, met, mop, thc, ket, mdma, bar, bup, bzo, mtd, and cardiac markers for troponin i & cardiac 3 in 1 (troponin i, myoglobin, ck-mb) and urine reagent rapid test, such as urs 1-12 parameters
Established: 2001
Verification Status
Contact Details:
Room 1017, Luohu
Shenzhen
518001
Guangdong
China
Turmeric is one of nature's most powerful healers. The active ingredient in turmeric is curcumin. Tumeric has been used for over 2500 years in India, where it was most likely first used as a dye.
The medicinal properties of this spice have been slowly revealing themselves over the centuries. Long known for its anti-inflammatory properties, recent research has revealed that turmeric is a natural wonder, proving beneficial in the treatment of many different health conditions from cancer to Alzheimer's disease.
Here are 20 reasons to add turmeric to your diet:
1. It is a natural antiseptic and antibacterial agent, useful in disinfecting cuts and burns.
2. When combined with cauliflower, it has shown to prevent prostate cancer and stop the growth of existing prostate cancer.
3. Prevented breast cancer from spreading to the lungs in mice.
4. May prevent melanoma and cause existing melanoma cells to commit suicide.
5. Reduces the risk of childhood leukemia.
6. Is a natural liver detoxifier.
7. May prevent and slow the progression of Alzheimer's disease by removing amyloyd plaque buildup in the brain.
8. May prevent metastases from occurring in many different forms of cancer.
9. It is a potent natural anti-inflammatory that works as well as many anti-inflammatory drugs but without the side effects.
10. Has shown promise in slowing the progression of multiple sclerosis in mice.
11. Is a natural painkiller and cox-2 inhibitor.
12. May aid in fat metabolism and help in weight management.
13. Has long been used in Chinese medicine as a treatment for depression.
14. Because of its anti-inflammatory properties, it is a natural treatment for arthritis and rheumatoid arthritis.
15. Boosts the effects of chemo drug paclitaxel and reduces its side effects.
16. Promising studies are underway on the effects of turmeric on pancreatic cancer.
17. Studies are ongoing in the positive effects of turmeric on multiple myeloma.
18. Has been shown to stop the growth of new blood vessels in tumors.
19. Speeds up wound healing and assists in remodeling of damaged skin.
20. May help in the treatment of psoriasis and other inflammatory skin conditions.
1. Buyer issues an official ICPO with the seller's procedure, passport copy, banking details along
with their Tank Storage Agreement "TSA".
2. Seller issues their Commercial Invoice "CI" to the buyer, Buyer signs and returns the commercial
invoice to the seller along with an Acceptance Letter of the sales and purchase procedure.
3. Seller verifies the buyer's storage facility and their Tank Storage Agreement (TSA) with the port
authority. (NB: Seller will issue a Tank-to-Tank Injection Agreement (TTIA) to be signed by all
parties only if buyer's TSA is engaged, not active or cannot be verified with the local port
authority).
4. Seller issues all POP documents below to the buyer upon a successful verification and approval
of the buyer TSA or after receiving the TTIA fully signed by all parties:
a. Injection Report.
b. Product Passport.
c. 24 Hours SGS Report.
d. Product Certificate of Origin.
e. Tank Storage Receipt (TSR).
f. Authorization to sell and collect.
g. Unconditional Dip-Test Authorization.
h. Product Title Holder Transfer Agreement.
i. NCNDA/IMFPA.
5. If required buyer may inspect by SGS (Dip Test In Tanks) at buyer's expense.
6. Upon successful verification of POP or Dip Test in the seller's tank, buyer provides Tank Storage
Receipt (TSR) to seller in order to issue the scheduled Injection Programming (IP) to be signed by
buyer storage facility and then injects the product into buyer's tanks.
7. Buyer makes the payment for the product via MT103, seller transfers the Title Holder &
Ownership of the product to the Buyer.
8. After successful Trial Lift (First Lift), Seller issues SPA/Contract for 12 months with R&E to
Buyer for processing.
9. Seller pays commissions to all intermediaries involved, for the initial lift and all subsequent lifts
according to the signed NCNDA/IMFPA.
COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold) comes in packs of 40 tests and contains:
GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request.
To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away.
1. Nasopharyngeal
2. Nasal
3. Saliva
Price and Minumum Quantity
Price FOB in USD: negotiable 0.8 to 1.8Minimum Order Qty: None Pieces
Production Capacity: 3,000,000/monthPackaging: 20 Tests/kit, 30 Kits/box, 12 Boxes/pallet
Sample: Available. Sample Cost Born By Supplier
Product Model And Origin
Brand: GENEDIAModel: 643G-S (Saliva)
Seller Code: Genedia w covid 19 agHS Code: 3002.15
Standards: Ce
Competitive Advantages
Allow wider testing with fast test time (10 minutes)
All necessary materials provided / no equipment needed
Sensitivity: 93.33%, specificity: 100%
Free sample. no moq. price is negotiable. customized packing.
Other Details
20 tests / kit
24 months from the date of manufacture
2 ~ 30c(35.6 ~ 86f) available for room temperature deliver
In stock. fast delivery.
1 x Instructions for Use Manual
40 x Test Cassettes
1 x Buffer
40 x Dropper
Basic Parameters
Dimensions: 201 x 99 x 35 mm
Weight: 333g
Adapter Input: AC 100 ~ 240 V Output: DC 24V 2.65A
Display mode
Segment LCD with white backlight + LED in red and green
Function Introduction
Charge
Active, pre-charge, constant current and constant voltages are the stages of charging mode. The initial charging mode depends on the battery voltage, so active and pre-charge don't happen to every batteries. For charging mode and current, please refer to the paragraphs of charging mode and charging current on page 2 & 3.
Tester will stop charging if one of the conditions below was met.
1) Remaining capacity 99% & current intensity = 0
2) Remaining capacity = full charge capacity
3) Current intensity reduce to end charge current when constant voltage charge
4) Remaining capacity reach up the set value
Discharge
Constant current discharge for double loads
Inner load: 0 ~ 1000mA, adjustable continuously via Battery Manager
External load: 0mA, 500mA, 1000mA, 1500mA, 2000mA, five gears with dip switches offered
Tester will stop discharging if one of the conditions below is met.
1) Remaining capacity set value
2) Voltage set value
3) Current intensity reduce to zero
Remarks:
Many batteries can not measure exact current intensity, which cause an else current value appears after you set a value. However, the actual discharging current is the same with your set value.
Test
Testing time is 12 seconds and the purpose is to check both the charging and discharging performances. After finishing test, LED flickers with green color and LCD reports the test result.
Normal: Test OK Shown on LCD
Abnormal: Test NG Shown on LCD
Possible causes and solutions for the abnormal:
1) Cause: battery voltage is too low to discharge
Solution: try to charge the battery to raise voltage
2) Cause: remaining capacity is too full to charge any more
Solution: try to discharge the battery to reduce the remaining capacity
3) Bad contact of battery connecting wires
4) Damaged battery
5) Tester trouble
Capacity Correction
The battery capacity value in the battery management chip will different from the actual capacity after a battery goes through many recycling cycles. It will affect the use of the battery when the difference reaches a certain degree. Capacity correction is to deep discharge a battery and then fully charge, which will correct the capacity value in the battery management chip.
Remarks:
Discharging current can be set via Battery Manager. Deep discharge will cause a battery losing communication with tester, so battery dropping phenomenon may happen in the discharging process if the end capacity and voltage are set too low. In such a case, active charge will make the battery work again.
50% Capacity
CD50%: charge firstly, and then discharge to 50% capacity
DC50%: discharge firstly, and then charge to 50% capacity
Online Functions
Tester can be connected with master machine via a USB port. Users can monitor, control and set parameters via Battery Manager software in the master machine.
Monitoring
Battery information can be monitored via three windows.
1. Home screen
Battery bar and brief information can be read on home screen.
2. Battery detail information window
Show smart battery data in real time and the data can be saved and printed in image format.
3. Battery graph window
Voltage, current and capacity are traced in curves.
Control
Battery Manager can control slave machine completely. Right-click menu on the battery bar includes the related commands.
Attention
All the functions of charge, discharge, capacity correction and 50% capacity are comply with the charging discharging conditions, which are showed on function introduction paragraph in page 4 & 5, so parameters should be set reasonably. Especially, deep discharge will cause a battery losing communication with tester.
Others
1. Active cooling
2. Active batteries of zero voltage
When a battery is deep discharged, the discharge protection circuit will start up and the voltage in the battery connector will become zero voltage. In this case, an appropriate voltage should be supplied to active the battery.
3. Battery identification
Battery information can be read from battery management chip after establishing communication.
4. Intelligent protection
Against over-current, over-voltage, over-charge, over-heat and short circuit.
5. Fan
Discharging mode: fan startup
Other modes: fan startup when temperature above 48
Fan stop working when temperature below 40
6. Trouble alarm
LED flickers in red color and current command stops when one of the conditions below happen.
1). There is not current for around 50 seconds when charge.
2). There is not current for around 25 seconds when discharge.
3). Charging time is above 8.8 hours.
4). Discharging time is above 9.9 hours.
5). Suitable for almost all laptop batteries, above 95%
Structure
Accessories
1).1 * adapter
2). 1 * USB cord
3). 1 * CD
4). 13 * connectors
5). 10 * cables
6). 10 * jumpers
7). 1 * loader
NON-NEGOTIABLE PROCEDURE FOR FOB TANK TO TANK (ACTIVE TSR)
1. The buyer issue ICPO with his international passport copy (data page), CIS and company
license to the seller.
2. The seller issue commercial invoice (CI) for the available quantity in seller storage tank to
the buyer, buyer endorse commercial invoice and return the CI with buyer signed tank
storage agreement.
3. Seller proceeds to verify the buyer's tank storage agreement to ensure seller approval of
the tank storage agreement through ATV, NCNDA/IMFPA signed and seal by all
intermediaries connected in the transaction.
4. The seller issues the partial pop documents as below and sends to the buyer.
a. Commitment to supply
b. Certificate of origin
c. Authorization to verify (ATV)
d. Tank to tank injection agreement (TTTIA)
e. Unconditional DTA
f. Fresh SGS (not older than 48 hours)
g. Tank storage agreement (TSR)
h. ATS- authorization to sell and collect
i. Injection report
5. The buyer conduct's DIP test in the seller reservoir and provides tank details to the seller,
to commence injection of product into the buyer's tank.
6. Within twenty-four (24) hours, buyer issues 100% TT wire transfer payment to the seller,
the seller transfers the title ownership to the buyer.
7. Serious direct buyers only, Please
General Information
Items : MOR/MET/THC/AMP/MDMA/MTD/COC/TCA/BAR/BZO, up to 15 kinds of Drug Tests
Format: Strip, Cassette, Cup,and Panel
Specimen: Urine
Packaging Details:
Pouch+Box+Carton packaging
The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.
PRECAUTION
1.For in vitro diagnostic uses only.
2.All patient samples should be treated as if capable of transmitting diseases.
3.Do not use test kit beyond expiration date.
4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
SUMMARY AND EXPLANATION OF THE TEST
It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.
PRINCIPLE
HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
One-Step Troponin I /CK-MB/ Myoglobin Rapid Test is intended for the qualitative determination of cardiac disease in human serum, plasma or whole blood.
