Please click here to check who's online and chat with them.

Sartron Biotechnology

Supplier From Turkey
Aug-02-20
Supplier : 1) Vnat Transfer tube (cat no: bs na 513) 2) itube (cat no: bs na 204) 3) direct rt qpcr sars cov 2 (cat no: bs sy sc2) 4) direct covid 19/flu rt qpcr (cat no: bs sy si) 5) direct covid 19/flu/rsv rt qpcr (cat no: bs sy sir) 6) direct respiratory tract rt qpcr mx 24t panel (cat no: bs sy mx24t)

Established: 2018

Verification Status



Contact Details:
Dumlupnar Bulvar Next Level 3A/81
Ankara 06510
Turkey


Recent User Reviews

This user has not received any reviews yet!
 
 
Contact Supplier
Renew

More Items Similiar to: Sartron Biotechnology

Aug-04-20
 
i) Used for sample-to-result SARS-CoV-2 detection in less than 60 minutes with only 3 minutes hands on time
ii) There is no need for any instrument other than real-time PCR devices such as nucleic acid extraction robots, microcentrifuges and incubators.
iii) Compatible with wide range of real-time PCR instruments produced by Roche, Bio-Rad, Qiagen, Thermo and BMS.
GOLD Member
May-16-21
Supplier From Saint-Paul, France
 
FINGERTIP PULSE OXIMETER

Parameters:

Two parameters:SPO2, Pulse Rate.



Waveforms:

SpO2 Waveform.



Features:

1 COLOR OLED display, four direction adjustable.

2 SpO2 and pulse monitoring, and Waveform display.

3 With menu operation.

4 With beep and alarm.

5 Low-power consumption, continuously work for 50 hours.

6 Small in size, light in weight, and convenient to carry.

7 Low voltage alarm display, Auto power-off.

8 Runs on standard AAA batteries.

Detailed descriptions of product functions:

SPO2:

1 Measurement range: 70%-99%

2 Accuracy: �±2% on the stage of 70%-99%, unspecified(<70%) for SPO2

3 Resolution: �±1%

4 Low perfusion: <0.4%

PR:

1 Measurement: range:30BPM-240BPM

2 Accuracy: �±1BPM or �±1%(the larger one)

3 Power: two AAA 1.5V alkaline batteries

4 Power consumption: below 30mA

5 Automatic power-off: the product shuts down automatically after no signal for 8 seconds
VERIFIED
May-22-20
Supplier From Seoul, South Korea (Republic Of Korea)
 
We are the authorized distributing partner of the South Korean diagnostic manufacturer BioTNS.

Our role is to distribute in South Korea and overseas the Covid-19
RT-PCR PNA kits.

1 kit allows you to test 100 patients.

- CE approved
- US FDA approved

Contact us to receive your quotation.
VERIFIED
Sep-07-21
 
CareStart Covid-19 Antigen Test Kits-Rapid Test Kits
Worldwide Shipping

Lateral flow assay
Detect SARS-CoV-2 nucleocapsid protein antigen
Rapid results within 10-15 minutes
Intended at POC setting (i.e., inpatient care settings) by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation
For use under the Emergency Use Authorization (EUA) only
For in vitro diagnostic use only
For prescription use only
For use with direct anterior nasal and nasopharyngeal swab specimens


Clinical Performance

93.75% PPAa and 99.32% NPAb when used with a nasopharyngeal swab
87.18% PPAa and 100% NPAb when used with anterior nasal swab

aPPA: Positive Percent Agreement, bNPA: Negative Percent Agreement.
VERIFIED
Apr-07-21
Supplier From Singapore, Singapore
Nov-17-17
Supplier From Shenzhen, Guangdong, China
 
Feline Leukemia Test INTENDED USE
Feline Leukemia Virus AG Rapid Test is a sandwich lateral flow immunochromatographic assay for the
qualitative detection of Feline Leukemia Virus antigen in cat's blood.
Assay Time: 5-10 min
Sample: Serum,Plasma or Whole Blood

Feline Leukemia Test PRINCIPLE
Feline Leukemia Virus AG Rapid Test is based on sandwich lateral flow immunochromatographic assay. The
test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone.
When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the
test strip. If there is enough feline leukemia virus antigen in the sample, a visible T band will appear. The C
band should always appear after a sample is applied, indicating a valid result. By this means, the device can
accurately indicate the presence of feline leukemia virus antigen in the sample.

Feline Leukemia Test KIT COMPONENT
1. Foil pouches, each containing one cassette, one pipette and a desiccant
2. Assay buffer (2.0 mL)
3. Centrifugal tubes
4. Product Manual

Feline Leukemia Test TEST PROCEDURE
1. Take cat's blood, serum or plasma as sample.
2. Take out the cassette from the foil pouch and place it horizontally.
3. Drip 1 drop of sample and immediately drip 2 - 3 drops of assay buffer into the sample hole "S".
4. Interpret the result in 10-15 minutes. Result after 15 minutes is considered as invalid.
Nov-17-17
Supplier From Shenzhen, Guangdong, China
 
INTENDED USE

Feline Panleucopenia Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Panleucopenia Virus (FPV Ag) in cat's feces or vomit.

PRINCIPLE OF THE ASSAY

Feline Panleucopenia Virus(FPV) Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Panleucopenia Virus antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Panleucopenia Virus antigen in the sample.

INTERPRETATION OF RESULTS

Positive: The presence of both C band and T band, no matter T band is clear or vague.

Negative: Only clear C band appears.

Invalid: No colored band appears in C zone, no matter whether T band appears.

STORAGE

The kit can be stored at room temperature (2-30�°C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.
Nov-17-17
Supplier From Shenzhen, Guangdong, China
 
INTENDED USE

Feline Immunodeficiency Virus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Immunodeficiency Virus antibody (FIV Ab) in cat's blood.

PRINCIPLE OF THE ASSAY

Feline Immunodeficiency Virus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody in the sample.

INTERPRETATION OF RESULTS

Positive: The presence of both C band and T band, no matter T band is clear or vague.

Negative: Only clear C band appears.

Invalid: No colored band appears in C zone, no matter whether T band appears.

STORAGE

The kit can be stored at room temperature (2-30C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.
Nov-17-17
Supplier From Shenzhen, Guangdong, China
 
1. INTENDED USE

FIV Ab + FeLV Ag Combined Rapid Test is a combined cassette to differentially diagnose the presence of Feline Immunodeficiency antibody and Feline Leukemia Virus antigen in cat's blood.

Assay Time: 10-15 min

Sample: serum, plasma or whole blood

2. PRINCIPLE OF THE ASSAY

FIV Ab + FeLV Ag Combined Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody or FeLV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody or FeLV antigen in the sample.

3. KIT COMPONENT

- 10 foil pouches, each containing a cassette,pipette and desiccant

- 10 assay buffer tubes (0.5 mL each)

- 10 centrifugal tubes

- Product Manual

Verification Status