Reszon Pregnancy Rapid Test Kit Midstream

Reszon Pregnancy Rapid Test Kit Midstream

Early detection: The right start for you and your baby!

RM19.90

RESZON Pregnancy Rapid Test Midstream is a rapid, one-step method to detect the Human Chorionic Gonadotropin (hCG) hormone in urine samples. It is designed for the early detection of pregnancy, making it suitable for convenient home self-testing.

  • Ultra-sensitive (detects pregnancy up to 5 days before your expected period)
  • Over 99% accurate
  • Results in 3 minutes

 

Product Registration: IVDB3556123-155383

Positive (Pregnant) - Pink-purplish band appears at the "C" region and ''T" region.
Negative (Not Pregnant) - Only one pink-purplish colored band appears at the "C" region.
Invalid - Absence of band in both regions, or only one band at the ''T" region is an indication of procedure error and/or the midstream test device has deteriorated. Repeat the assay using a new midstream test device.

1. When you are ready to test, tear the foil pouch at the notch and remove the midstream test device from the pouch.
2. Take the cap off.
3. Hold the midstream test device above the thumb grip at 45° angle / slanting position while peeing directly on it for 15 seconds. Alternatively, you could also collect urine in a clean, dry container / cup & dip the sample pad area in the cup for 15 seconds.
4. Remove the midstream test device from urine. Put the cap on & keep the device on a clean, flat surface.
5. Read results after 3 minutes.

1. How does the test work?
The Reszon Pregnancy Rapid Test Midstream (10 mlU/ml) is a one-step pregnancy test that detects the presence of a hormone called human chorionic gonadotropin (hCG) in urine. It employs a combination of antibodies to accurately identify hCG in urine samples with high sensitivity.

1. Do I have to test with first morning urine?
Yes. You can test at any time of the day, however, the first morning urine generally contains the highest concentration of hormone.

2. How accurate is the test?
The test is more than 99% accurate in clinical tests when used from the day of expected period.

3. How do I know whether the test was run properly?
The control line should appear which shows that you have followed the test procedure properly and the proper amount of urine was absorbed.

4. Can any medication or medical conditions affect the result?
Fertility drugs that contain hCG may cause misleading and false positive result.

5. Why is it advised against consuming large amounts of fluids before taking the test?
Drinking large amounts of fluids before using the test can dilute the concentration of the pregnancy hormone (hCG) in urine, potentially leading to inaccurate results, specifically false negatives.

6. How do you store the Reszon Pregnancy Rapid Test?
Store at 4-30 °C, do not freeze. Keep the test device sealed until used. Keep away from direct sunlight, moisture and heat.

7. What are the levels of hCG that the Reszon Pregnancy Rapid Test can detect?
Elevated levels of hCG equal to or greater than 10 milli-lnternational Units per milliliter (mlU/ml) can be detected in less than 5 minutes. This level of hCG concentration can be detected as early as 5 days before a missed period, though it's important to note that hormone levels can vary between individuals.

8. Why is the sample pad covered and not exposed like other market brands?
The entire test strip, comprising the sample pad area, membrane area, and absorbent pad, is enclosed within a plastic housing to safeguard it from physical damage. Small openings in the sample pad area allow for the gradual absorption of urine, preventing a "flushing effect" that could cause the urine sample to move too quickly and potentially affect the reaction in the test area.

9. Why does the Reszon Pregnancy Rapid Test recommend a 15-second urine stream duration, whereas other brands typically suggest 5-10 seconds?
The Reszon Pregnancy Rapid Test will still function properly when exposed to the urine stream or immersed in the urine sample for 10-15 seconds. We recommend a 15-second duration in the Instructions for Use (IFU) to ensure that an adequate urine sample is applied for accurate results.