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CITEST DIAGNOSTICS INC.

  • China,Hangzhou ,Zhejiang
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China One Step 500ng/Ml Fast Reading Drug Of Abuse Test Kit For Carfen/tanyl CFYL
China One Step 500ng/Ml Fast Reading Drug Of Abuse Test Kit For Carfen/tanyl CFYL

  1. China One Step 500ng/Ml Fast Reading Drug Of Abuse Test Kit For Carfen/tanyl CFYL
  2. China One Step 500ng/Ml Fast Reading Drug Of Abuse Test Kit For Carfen/tanyl CFYL
  3. China One Step 500ng/Ml Fast Reading Drug Of Abuse Test Kit For Carfen/tanyl CFYL

One Step 500ng/Ml Fast Reading Drug Of Abuse Test Kit For Carfen/tanyl CFYL

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Supply Ability 10 M tests/month
Delivery Time 2-4 Weeks
Packaging Details 25T/40T/50T
Product Carfen/tanyl CFYL One Step 500ng / Ml Fast Reading Drug Of Abuse Diagnosis Test Kit
Cat. No. DCFY-X14
Principle Chromatographic Immunoassay
Format Dipstick, Cassette, Panel, Device, Cup
Specimen Urine, Oral Fluid, Powder
Certificate CE
Reading Time 5 minutes
Pack 25T/40T/50T
Storage Temperature 2-30°C
Shelf Life 2 Years
Sensitivity 94.7%
Specificity 98.6%
Accuracy 97.3%
Cut-Off 500 ng/mL*, 250 ng/mL, 50 ng/mL*
Brand Name Citest
Model Number DCFY-X14
Certification CE, ISO13485
Place of Origin -

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  1. Product Details
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Product Specification

Supply Ability 10 M tests/month Delivery Time 2-4 Weeks
Packaging Details 25T/40T/50T Product Carfen/tanyl CFYL One Step 500ng / Ml Fast Reading Drug Of Abuse Diagnosis Test Kit
Cat. No. DCFY-X14 Principle Chromatographic Immunoassay
Format Dipstick, Cassette, Panel, Device, Cup Specimen Urine, Oral Fluid, Powder
Certificate CE Reading Time 5 minutes
Pack 25T/40T/50T Storage Temperature 2-30°C
Shelf Life 2 Years Sensitivity 94.7%
Specificity 98.6% Accuracy 97.3%
Cut-Off 500 ng/mL*, 250 ng/mL, 50 ng/mL* Brand Name Citest
Model Number DCFY-X14 Certification CE, ISO13485
Place of Origin -
High Light Fast Reading Drug Of Abuse Test Kit500ng/Ml Drug Of Abuse Test KitOne Step Test Kit For Carfentanyl

CE Mark Carfen/tanyl (CFYL) One Step  500ng/ml Fast Reading  Drug of Abuse Diagnosis Test Kit Test Panel Powder 

 

Product features Parameters
Principle Chromatographic Immunoassay
Format Dipstick, Cassette, Panel, Device, Cup
Specimen Urine, Oral Fluid, Powder
Certificate CE
Reading Time 5 minutes
Pack 25T/40T/50T
Storage Temperature 2-30°C
Shelf Life 2 Years
Sensitivity 94.70%
Specificity 98.60%
Accuracy 97.30%
Cut-Off 500 ng/mL*, 250 ng/mL, 50 ng/mL*

 

Application:

 

The Carfen/tanyl (CFYL) Rapid Test Panel (Powder) is a rapid immunochromatographic assay for the qualitative detection of carfe/ntanyl. This test will detect other compounds, please refer to Analytical Specificity table in this package insert.


This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

 

Description:  

 

Carfe/ntanyl is an analog of the synthetic opioid analgesic fen/tanyl. It is 10,000 times more potent than morp/hine, making it among the most potent commercially used opioids. Carfenta/nyl was first synthesized in 1974. It is marketed under the trade name Wild/nil as a general anaesthetic agent for large animals. Side effects of carfe/ntanyl are similar to those of fen/tanyl, which include itching, nausea and respiratory depression, which can be life-threatening. Carfen/tanyl is classified as Schedule II under the Controlled Substances Act in the United States with a DEA ACSCN of 9743.
 
The Carf/entanyl (CFYL) Rapid Test Panel (Powder) is a rapid Powder screening test that can be performed without the use of an instrument. The test utilizes a monoclonal antibody to selectively detect elevated levels of Carfe/ntanyl. The Carfe/ntanyl (CFYL) Rapid Test Panel (Powder) yields a positive result when the concentration of Carfen/tanyl exceeds 500 ng/ml.

 

How to use?

 

Test device (in closed pouches), samples, and controls should be brought to room temperature (15-30°C) prior to testing. Do not open pouches until ready to perform the assay. Remove the test device from its protective pouch and label the device with patient’s identification or control label.
 
FOR SURFACES
 
1. Wipe with the Sample marked side of strip in the panel over the surface on which the drugs are suspected.
 
2. Take off the cap of buffer vial.
 
3. Fill all buffer from the buffer vial into the protection cover.
 
4. Insert the Test slowly and carefully into the protection cover with buffer.
 
5. Wait for control line to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.
 

 
FOR SOLIDS WITHOUT SWAB
 
1. Open the buffer vial and put a pinch of suspected solid in to the buffer.
 
2. Close the vial with dropper and cap. Shake it vigorously for a short time. Wait for 30sec.
 
3. Take off the cap of dropper cap.
 
4. Fill all the buffer with dissolved substances into the protection cover.
 
5. Insert the Test slowly and carefully into the protection cover with buffer.
 
6. Wait for control line to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.
 

 
 
FOR SOLIDS WITH SWAB
 
1. Take out the buffer vial and open the lid. Place the swab into the tube for 5-10 seconds to allow swab head to be thoroughly soaked in the buffer.
 
2. Take out the swab and wipe the surface solids gently at least 3 times, and then insert the swab intobuffer vial and mix well for at least 1 minute. Squeeze the swab several times by compressing the outside walls of the vial against the swab to mix well. Finally squeeze the swab to make most of the solution stay in the buffer vial and remove the swab. Use solution thus obtained as specimen.
 
3. Take off the cap of dropper cap.
 
4. Fill the solution with dissolved substances into the protection cover.
 
5. Insert the Test Panel slowly and carefully into the protection cover with buffer.
 
6. Wait for control line to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.
 

 

 

INTERPRETATION OF RESULTS


(Please refer to the illustration above)

NEGATIVE:* A colored line appears in the Control region (C) and colored lines appear in the Test region (T). This negative result means that the concentrations in the sample are below the designated cut-off levels for a particular drug tested.


*NOTE: The shade of the colored lines(s) in the Test region (T) may vary. The result should be considered negative whenever there is even a faint line.

POSITIVE: A colored line appears in the Control region (C) and NO line appears in the Test region (T). The positive result means that the drug concentration in the sample is greater than the designated cut-off for a specific drug.


 

INVALID: No line appears in the Control region (C). Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for Control line failure. Read the directions again and repeat the test with a new test card. If the result is still invalid, contact your manufacturer.

 

Order Information

 

Cat. No. Product Specimen Pack
DCFY-102 Carfe/ntanyl (CFYL) Rapid Tests Cassette Urine 40T
DCFY-114 Carfe/ntanyl(CFYL) Rapid Tests Panel Urine 40T
DCFY-101 Carfe/ntanyl(CFYL) Rapid Tests Dipstick Urine 50 T
DCFY-802 Carfe/ntanyl(CFYL) Rapid Test Cassette Oral Fluid 25 T
DCFY-803 Carfe/ntanyl(CFYL) Rapid Test Device Oral Fluid 25T
DCFY-X14 Carfe/ntanyl(CFYL) Rapid Test Panel Powder 25T

Company Details

Bronze Gleitlager

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Bronze Sleeve Bushings

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Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer,Exporter,Trading Company

  • Total Annual:

    80000000-100000000

  • Employee Number:

    500~10000

  • Ecer Certification:

    Verified Supplier

CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ... CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ...

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Get in touch with us

  • Reach Us
  • CITEST DIAGNOSTICS INC.
  • 170-422, Richards Street, Vancouver BC V6B 2Z4, CANADA
  • https://www.citesttestkit.com/

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