Opioid analgesics is made up of a variety of inhibiting substance
that inhibit the central nervous system. may lead to tolerance and
physical . Usually it can be detected after that someone has taken
a few days. The test kit is one of urine test kits that no need any
devices or equipment, use immuno chromatographic techniques to
qualitatively detect in urine.
Product details
Description
Delivery
Within 48 hours
Packaging Specifications
25 piece/box
Country Of Origin
China
Manufacturer
24months
Preservation method
2℃-30℃
Specimen
urine
Assification
class1
Type
Reply Test
Test Methods
Place the reagent at room temperature for 30 minutes before use,
and return to room temperature(20℃-30℃. Instructions must be read
entirely before taking the test. Do not open the inner packaging
until ready, it must be used as soon as possible if
opend(Humidity:20%~90%,Temp:10℃-50℃).
1. Strip: Remove the test device from the sealed pouch, put the end of the
test strip print with arrow into the specimen (about 50-60μl), the
interface of urine should not exceed the MAX line, take it out
after 5s and place the test stripe on a clean and level surface.
Cassette: Take off the outer packing, put the cassette onto the desk with
the sample window up.Drop 3 drops of specimen (100μl) vertically
into the circular groove of cassette.
2. Observe the test results immediately within 5-10 minutes, the
result is invalid over 10 minutes.
Storage
Store as packaged in the sealed pouch at 4-30°C, avoid hot and
sunshine, dry place, valid for 24 months.
DO NOT FREEZE. Some protective measures should be taken in hot
summer and cold winter to avoid high temperature or freeze-thaw.
Company Profile
Biovantion Inc is independent from international department of
Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro
diagnostic reagents manufacturer engaged in the research,
development, production, and focus on clinical testing for
infectious diseases, such as Hepatitis virus, Noro virus, Parvo
virus test kits, our products include rapid test cassette and Elisa
kits.
All our products have been registered in National Medical Products
Administration of China, in year 2020 we get Certificate of ISO
13485:2016 – QUALITY MANAGEMENT SYSTEMS FOR MEDICAL DEVICES from
SGS. More importantly, we have awarded the registration certificate
from National Medical Products Administration for Diagnostic Kit
for IgM Antibody to COVID-19 and IgG antibody to COVID-19 during
the outbreak in China, and also we developed COVID-19 Antigen test
; Neutralizing Antibody Test, these products selling well all
overthe world
For Laboratory Or Hospital High Accuracy MOP) Rapid Test Kit