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Tilidine TLD Drug Abuse Cassette Rapid Test High Sensitivity Diagnostic Kit

Basic Information
Place of Origin: CHINA
Brand Name: AllTest
Certification: CE, FDA 510K
Model Number: DTLD--101/DTLD--102/DTLD--114
Minimum Order Quantity: 500
Packaging Details: 50T/Kit
Supply Ability: 100 Million a year
Format: Dipstick/Cassettte/Panel Specimen: Urine
Kit Size: 50T/Kit Cut-Off: 50 Ng/mL
Color: Yellow Certificate: CE
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A rapid test for the qualitative detection of Tilidine (TLD)​ in human urine. For professional in vitro diagnostic CE certified

 

 

Applications And Description:

 

Tilidine (TLD), or tilidate (brand names: Tilidin, Valoron and Valtran) is a synthetic opioid painkiller, used mainly in Germany, Switzerland, South Africa and Belgium for treatment of moderate to severe pain, both acute and chronic. Its onset of pain relief after oral administration is about 10–15 minutes and peak relief from pain occurs about 25–50 minutes after oral administration.
The TLD Rapid Test (Urine) is a rapid urine-screening test that can be performed without the use of an instrument. The test utilizes the antibody to selectively detect elevated levels of Nortilidine in urine.

 

How to use?

Allow the test, urine specimen, and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it within one hour.
2. Place the test cassette on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 120μL) to the specimen well (S) of the test cassette, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration below.
3. Wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10minutes.

Tilidine TLD Drug Abuse Cassette Rapid Test High Sensitivity Diagnostic Kit 0

【DIRECTIONS FOR PANEL USE】
Allow the test, urine specimen, and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test panel from the sealed pouch and use it within one hour.
2. Remove the cap.
3. With the arrow pointing toward the urine specimen, immerse the test panel vertically in the urine specimen for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.
4. Replace the cap and place the test panel on a non-absorbent flat surface.
5. Start the timer and wait for the colored line(s) to appear.
6. The result should be read at 5 minutes. Do not interpret the result after 10 minutes.

Tilidine TLD Drug Abuse Cassette Rapid Test High Sensitivity Diagnostic Kit 1

【DIRECTIONS FOR DIPSTICK USE】
Allow the test, urine specimen, and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test dipstick from the sealed pouch and use it within one hour.
2. With arrows pointing toward the urine specimen, immerse the test dipstick vertically in the urine specimen for at least 10-15 seconds. Do not pass the maximum line (MAX) on the Test Dipstick when immersing the strip. See the illustration below.
3. Place the test dipstick on a non-absorbent flat surface, start the timer and wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10 minutes.

Tilidine TLD Drug Abuse Cassette Rapid Test High Sensitivity Diagnostic Kit 2

 

 

 

INTERPRETATION OF RESULTS

 

(Please refer to the illustration above)

 

NEGATIVE:* Two lines appear. One color line should be in the control region (C), and another apparent color line should be in the test region (T). This negative result indicates that the Tramadol (TML) concentration is below the detectable cutoff level.

 

*NOTE: The shade of color in the test region (T) may vary, but it should be considered negative whenever there is even a faint color line.

 

POSITIVE: One color line appears in the control region (C). No line appears in the test region (T). This positive result indicates that the Tilidine (TLD) concentration is above the detectable cutoff level.

 

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test Dipstick. If the problem persists, discontinue using the test Dipstick immediately and contact your local distributor.

 

 

Cat. No. Product Description Specimen Format Kit Size Cut-Off Status
DTLD-102 Tilidine (TLD) Rapid Test Cassette Urine Cassette 40 T 50 ng/mL* CE
DTLD-114 Tilidine (TLD) Rapid Test Panel Urine Panel 40 T CE
DTLD-101 Tilidine (TLD) Rapid Test Dipstick Urine Dipstick 50 T CE

 

 

 

Contact Details
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