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Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml

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Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml

China Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml supplier
Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml supplier Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml supplier

Large Image :  Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml

Product Details:

Place of Origin: China
Brand Name: New Life
Certification: ISO13485, CE
Model Number: PPX

Payment & Shipping Terms:

Minimum Order Quantity: 5000pcs
Price: USD0.5-USD5
Packaging Details: 1pc/pouch, 25pcs/box
Delivery Time: 20-30days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 2000000pcs/month
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Detailed Product Description
Category: Drug Abuse TESGTING Kits Format: CARD 4 PPX
Specimen: Urine Testing Time: 5-15
Shelf Life: 24 Months Application: Ppx ABUSE Test
Cut-off: 300ng

Propoxyphene (PPX) Drug Abuse Test Kit PPX Rapid Test 4mm dipcard , cut-off 300ng/Ml

 

Product Name

 

Propoxyphene (PPX) Drug Abuse Test Kit

Specimen: Urine

 

 

Intended Use

 

The Propoxyphene Assay is intended for qualitative determination of propoxyphene in human urine.

 

This assay provides only a preliminary analytical test result. A more specific alternative 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.

 

Parameter Calibrator Cut-off (ng/mL)
PPX Propoxyphene 300

 

 

 

 

 

 

 

 

Test Principle

 

Reagent Preparation and Storage The reagents are ready for use. No reagent preparation is required. All assay components, when stored properly at 2-8°C, are stable until the expiration date indicated on the label.

In the case of accidental spill, clean and dispose of material according to your laboratory’s SOP, local, and state regulations.

In the case of damaged packaging on arrival, contact your technical support representative (refer to back page of this PI).

 

DIRECTIONS FOR USE

 

Collect urine specimens in clean glass or plastic containers. Testing fresh urine specimens is suggested.

 

The Mandatory Guidelines for Federal Workplace Drug Testing Programs recommends that specimens that do not receive an initial test within 7 days of arrival at the laboratory should be placed into secure refrigeration units.

 

Samples within a pH range of 3 to 11 are suitable for testing with this assay.

 

An effort should be made to keep pipetted samples free of gross debris. It is recommended that highly turbid specimens be centrifuged before analysis. Adulteration of the urine sample may cause erroneous results. If adulteration is suspected, obtain another sample and forward both specimens to the laboratory for testing.

 

 

INTERPRETATION OF RESULTS

 

 

NEGATIVE:* A colored line appears in the Control region (C) and colored lines appears in the Test region (T). This negative result means that the concentrations in the urine 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 urine 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.

 

 

QUALITY CONTROL

 

A procedural control is included in the test. A colored line appearing in the control line region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.

 

performance characteristics

 

A side-by-side comparison was conducted using the PPX Rapid Test Cassette (Urine) and GC/MS. The following results were tabulated:

 

 

Table 1: Specimen Correlation

 

 

Level Low Control Cutoff Cal High Control
       
Mean (mA/min) 324.4 379.7 422.5
       
Within-run SD (mA/min) 2.3 2.6 1.9
       
Within-run CV% 0.7 0.7 0.4
       
Total-run SD (mA/min) 5.3 5.4 5.4
       
Total-run CV% 1.6 1.4 1.3

 

 

Propoxyphene PPX Rapid Test 4mm Dipcard For Human Urine 300ng/Ml

 

ORIENT NEW LIFE MEDICAL CO., LTD.
Contact: Jerry Meng
Email: Jerry @ newlifebiotest .com
Tel. +86 18657312116
SKYPE enetjerry

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Contact Person: Jerry Meng

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