Specifications
Brand Name :
Newscen
Model Number :
HCG
Certification :
ISO9001, CE, TUV, FDA
Place of Origin :
China
MOQ :
10 Boxes or 400 Kits (40 Kits/Box)
Price :
USD0.45/Cassette
Payment Terms :
T/T, Western Union, MoneyGram
Supply Ability :
50,000 Kits Per Day
Delivery Time :
8 days
Packaging Details :
40 Kits/Box, 50 Boxes/Carton, 317g/Box, 18kgs/Carton, Box Size: 250x125x65mm, Carton Size: 650x510x330mm
Methodology :
Colloidal Gold
Format :
Cassette / Strip
Result Time :
Read in 20 Minutes
Usage :
For In Vitro Diagnostic Use Only
Manufacturer/Trader :
Manufacturer
OEM/ODM :
Acceptable
Description

Human Chorionic Gonadotropin (HCG) Tests (Pregnancy tests)

HCG Rapid Diagnostic Kit Pregnancy Test Fast Urine Detection Cassette In Vitro Test Colloidal Gold

Intended Use

Human Chorionic Gonadotropin (HCG) tests are single use, rapid immunoassay for in vitro qualitative determination of human chorionic gonadotropin (HCG) in urine to aid in the early detection of pregnancy. It is intended for use by the lay users.

In Vitro Pregnancy Rapid Test Kit

Principle

Antibodies to HCG are precoated onto membrane as a capture reagent on the test zone. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with antibodies to HCG. If HCG is present, a red colored line will develop on the membrane in proportion to the amount of HCG present in the specimen. To serve as a procedural control, red colored line in the control zone will always appear regardless of the presence of HCG.

In normal pregnancy, HCG can be detected in urine after fertilization. Usually, concentration of HCG in urine is at least 25mIU/ml as early as seven to ten days after conception. The concentration increases steadily and reaches its maximum between the eighth and eleventh weeks of pregnancy.

The appearance of HCG soon after conception and its subsequent rise in concentration during early gestational growth make it an excellent marker for the early detection of pregnancy

In Vitro Pregnancy Rapid Test Kit

Reagents and Materials Provided

Each kit contains:

Each pouch contains one cassette with one desiccant bag

Instruction for use

Urine cup

Disposable plastic dropper

Materials Required But Not Provided

Timer or stopwatch

In Vitro Pregnancy Rapid Test Kit

Sample Collection and Test Preparation

First morning urine typically contains the highest concentration of HCG and is therefore the best sample for performing the urine test. However, any urine specimen may be used.

Collect the urine specimen in a clean container. Do not use preservatives.

If the specimen is not used immediately following collection, but is to be used within 48 hours it should be refrigerated (2 to 8℃), and brought back to room temperature before testing. If the specimen is not going to be used for more than 48 hours, it should be frozen at -20℃. A frozen specimen should not be used if stored longer than 2 weeks. Prior to testing, the frozen specimen must be completely thawed, thoroughly mixed, and brought to room temperature.

Urine samples exhibiting visible precipitates should be filtered, centrifuged, or allowed to settle and clear aliquots obtained for testing.

Assay Procedure

Allow the test, urine specimen and/or controls to reach room temperature prior to testing.

Before opening, allow the test cassette to reach room temperature. Use it immediately after opening.

Place the test cassette on a dry, clean, non-absorbent flat surface, add 2-3 drops of urine into Sample well, and start the timer and wait for the colored line(s) to appear.

Read results at 1-5 minutes. Do not interpret the result after 10 minutes.

In Vitro Pregnancy Rapid Test Kit


Interpretation of Results

In Vitro Pregnancy Rapid Test Kit

Negative: No red lines appear within 10 minutes in the test zone (T), only a red line in the control zone (C), which this indicates that the specimen does not contain a detectable level of HCG.

Positive: One red line in the control zone (C) and one red line in the test zone (T). This indicates the specimen contains HCG.

Invalid: If no red lines appear, the test is invalid. Discard the test and repeat with new specimen and new cassette.

Built-In Control

Human Chorionic Gonadotropin (HCG) tests have a built in procedural control that demonstrates assay validity. A red line appearing adjacent to the control zone (C) indicates that the test runs correctly.

In Vitro Pregnancy Rapid Test Kit

Storage

Human Chorionic Gonadotropin (HCG) tests should be stored at room temperature (4-30℃, do not freeze) for 24 months from the date of manufacture. Keep the test cassette in sealed pouch until use. Once you have taken the test cassette out of the pouch, perform the test as early as possible (within 1 hour) to avoid test cassette from becoming moist.


Precision

Intra-assay: The test strips of the same lot number were used in the specimens containing 25mIU/mL hCG. Results and color are consistent.

Inter-assay: Three lots of test strips were used in specimens containing 25mIU/mL hCG. Results and color are consistent.

Clinical Study

The study included 80 positive and 120 negative patient urine specimens confirmed by routine diagnostic method and tested by pregnancy test strip. The results showed 100% consistency.

In Vitro Pregnancy Rapid Test Kit

In Vitro Pregnancy Rapid Test Kit

Send your message to this supplier
Send Now

In Vitro Pregnancy Rapid Test Kit

Ask Latest Price
Brand Name :
Newscen
Model Number :
HCG
Certification :
ISO9001, CE, TUV, FDA
Place of Origin :
China
MOQ :
10 Boxes or 400 Kits (40 Kits/Box)
Price :
USD0.45/Cassette
Contact Supplier
In Vitro Pregnancy Rapid Test Kit
In Vitro Pregnancy Rapid Test Kit
In Vitro Pregnancy Rapid Test Kit
In Vitro Pregnancy Rapid Test Kit

Newscen Biopharm Co., Limited

Active Member
5 Years
tianjin, tianjin
Since 2003
Business Type :
Manufacturer, Seller
Employee Number :
200~300
Certification Level :
Active Member
Contact Supplier
Submit Requirement