This reagent for the in vitro qualitative detection of human chorionic gonadotropin in urine of women (of HCG), for diagnosis of early pregnancy.
Storage conditions and period of validity
2°-30°C dry and cool, can not be frozen. Valid for 24 months, Use within 1 hours after opening.
Related type recommendation
Strip Type/ Cassette Type
Product Display
INTENDED USE
This reagent for the in vitro qualitative detection of human chorionic gonadotropin in urine of women (of HCG), for diagnosis of early pregnancy, can not be used for diagnosis of tumors.
SPECIMEN REQUIREMENTS
1. Urine specimens can be collected in a clean, dry container. Urine can be detected at any time, but recommended morning urine. Because the highest concentration of HCG in morning urine.
2. It is best to use fresh samples for testing, if not timely detection, should be placed in 2-8 ℃ refrigerator in the refrigerator, storage time 6-8 hours; for extended storage time, can be frozen below -20 ℃ , Avoid repeated freezing and thawing, frozen or frozen specimens should be fully restored before testing room temperature, shake. Do not shake or remove the supernatant when the turbidity and sedimentation occurs in the urine sample, or take the supernatant by centrifugation or filtration.
Testing Method
1. Dilacerate the aluminum foil pouch, then take out the LH Midstream test device, remove the cap to expose the absorbent tip, hold the test device and urinate directly in the absorbent tip about 3 seconds (Notice: Don’t urinate in the result window). Otherwise, you can collect your urine into a clean cup and dip half of the absorbent pad into the urine for at least 3 seconds.
2. Lay the midstream flatly on a non-absorbent clean surface start the timer and wait for the red line(s)to appear.
3. 3 minutes to observe the results,10 minutes after the results are invalid.
Do not read the test result more than 10 minutes or less than 3 minutes as it may change or become unreliable. To avoid confusion, discard the test device and the urine cup after establishing the test result.
Warning&precaution
1. This product is a one-time in vitro diagnostic reagents, urine cups and test strips can not be reused.
2. Test equipment is not clean or improper operation will produce the wrong results, please follow the instructions to test.
3. Beware of the damp, do not touch the reaction before use, to determine the use of packaging and then open.
4. Urine samples and used test paper as a contaminant, to avoid contact with the skin.Dispose of all potentially contaminated test components in a biohazard container.
5. There is a desiccant in the package.
6. The first test negative, the proposed 48 hours after the morning urine test.
7. suspected ectopic, abnormal pregnancy, should be combined with other methods for diagnosis.
8. Do not use test components beyond their expiration dates.
Why Choose us
1. 7-24 contact online
2. On-site laboratory test and control raw material and finished products
3. 100% original material offer
4. Free samples available
5. Flexible package offer
6. ODM/OEM, Registration service
7. CE&ISO Certification available
8. Top Quality and fast delivery
9. Professional technology team for after-sales service
Company information
Shenzhen GLD Biotechnology Ltd-Owned by Pharmatech Asia Group Ltd., was founded in 2000,as a professional manufacturer mainly producing medical device like pregnancy(HCG) and ovulation (LH) test and homecare medical like Compressor Neublizer Series , Blood Pressure Meter Series , Hearing Aid Series and other endocrine system product such as Digital Thermometer Series, Quantum Analyzer Series, Blood Glucose Series .
GLD , Located in Shenzhen City , Guangdong province, China, next to Hongkong, has its GMP standard plant and over 150 employees. For products in vitro diagnosis, We have a complete production line from parts to finished product, including plastic housing mould design and production, plastic housing production, test strip production and cutting, test midstream and cassette assembling, pouch printing, drying agent packing, and final package.
With a professional R&D, QA&QC team, GLD can well control every aspect of the product quality including raw material, semi-product and finished product. Therefore, GLD focuses to provide customer good products with controlled quality, cost and lead time. We also have ISO certificate and CE certificate for in vitro diagnosis products.
Welcome to visit us anytime.
Certificates
FAQ & Contact Us
1. Q: How much experience do your company have in this medical
device industry?
A: We have been manufacturing since 2000 and exporting medical
device products since 2008.
2. Q:How can you guarantee the quality?
A:We have full hi-tech equipment for test and QC check under high
standard QC system. And each product has to be 100%
inspected before shipment.
3. Q:What is the FOB price and CIF price
A:In general, our prices are given on a FOB basis. For CIF price, I will
check the cost from our shipping agent and recommend to
you.
4. Q:How can you guarantee the exclusive sale for OEM & ODM
