CLIA Waived Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests. This test is also authorized for use with fingerstick whole blood specimens only at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation. The COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only. Indication: Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. About Test Device EUA Authorized Gives Positive or Negative Result for COVID-19 virus Read Results in 15 Minutes 24 Month Expiration from Date of Manufacture Contents 20 Test Devices 20 Disposable Pipettes 20 Alcohol Prep Pads Sterile Safety Lancets Buffer Package Insert
COVID finger prick, rapid antigen test, or rapid test, is a rapid diagnostic test suitable for point-of-care testing that directly detects the presence or absence of an antigen. It is commonly used for the detection of SARS-CoV-2, the virus that causes COVID-19. Rapid tests are a type of lateral flow tests that detect protein, distinguishing it from other medical tests that detect antibodies or nucleic acid, of either laboratory or point-of-care types. Rapid tests generally give a result in 1 to 15 minutes, require minimal training or infrastructure, and have significant cost advantages. NO Lab Required for results.
SAVEWO 3DMASK is a disposable medical respirator, which fulfils the specifications of CE EN149:2001+A1:2009 FFP2 NR for filtering bacteria, viruses, and other harmful particles. Color: White, Blue, Green, Grey, Black Product compliances: EU Standard EN149:2001 + A1:2009 (FFP2 NR) EN14683:2019 Type IIR ASTM F2001-19 Level 3 KMOEL-2017-64 KF94 Tested by Nelson Laboratories / SGS /KOTITI ISO14644-1:1999 Class7 certified Cleanroom Production ISO13485:2016 Medical Device Quality Management System EU CE Certification US FDA Registration No: 3017178899
SAVEWO 3DMASK Extreme Pro is an innovative disposable medical respirator-which fulfill the specifications of CE EN149:2001+A1:2009 FFP3 NR (equivalent to N99 standard) for filtering bacteria, viruses, and other harmful particles. EU Standard EN149:2001 + A1:2009 (FFP3 NR) EN14683:2019 Type IIR ASTM F2001-19 Level 3 Tested by Nelson Laboratories / SGS /KOTITI ISO14644-1:1999 Class7 certified Cleanroom Production ISO13485:2016 Medical Device Quality Management System EU CE Certification US FDA Registration No: 3017178899
In fact, saffron sample grading depends on laboratory standards set for color, flavor and aroma, which means testing the major components crocin, picrocrocin and safranal through photospectroscopy. They must surpass a given ceiling in order to be considered even at the lowest or poorest category. Crocin, in particular, is the primary consideration because all other components are affected by its presence. Authentic saffron threads and powders are graded from I to IV, with I as the finest and IV the poorest. The following is the grading scale for crocin absorbance: 1. Grade I: >190 2. Grade II: >150 3. Grade III: >110 4. Grade IV: < 110
INTENDED USE UrineCheck 7 is a fast dip-and-read test for the determination of diluted or adulterated urine specimens. It is an important pre-screening test for any drug-testing program. Each bottle contains 25 strips. SUMMARY AND EXPLANATION UrineCheck 7 drug adulteration tests are firm plastic strips to which seven different reagent areas are affixed. UrineCheck 7 test strips are ready-to-use and disposable. No equipment is required for its use. Only fresh and uncentrifuged urine samples without preservatives are to be used. UrineCheck 7 provides tests for Creatinine, Nitrite, pH, Specific Gravity, Glutaraldehyde, Oxidants, and Pyridium Chlorochromate in urine. Test results may be useful for assessing the integrity of the urine sample prior to Drugs-of-Abuse testing; for example, whether the sample is possibly diluted with water or other liquids as indicated by the creatinine and specific gravity tests. UrineCheck 7 detects whether the sample contains commercially available adulterants including nitrite, glutaraldehyde, bleach, pyridinium chlorochromate and other oxidizing agents. UrineCheck 7 can also assess whether the sample is possibly contaminated by acidic (vinegar) or basic (ammonia solution) adulterants as indicated by the pH test.
Precision Dx - Adulteration Strips: Nitrite, Creatinine, Glutaraldehyde, PH, Specific Gravity, Oxidants, Pyridium Chlorochromate 25/Bottle INTENDED USE PrecisionDX is a fast dip-and-read test for the determination of diluted or adulterated urine specimens. It is an important pre-screening test for any drug-testing program. Each bottle contains 25 strips. SUMMARY AND EXPLANATION PrecisionDx drug adulteration tests are firm plastic strips to which seven different reagent areas are affixed. PrecisionDX test strips are ready-to-use and disposable. No equipment is required for its use. Only fresh and uncentrifuged urine samples without preservatives are to be used. PrecisionDX provides tests for Creatinine, Nitrite, pH, Specific Gravity, Glutaraldehyde, Oxidants, and Pyridium Chlorochromate in urine. Test results may be useful for assessing the integrity of the urine sample prior to Drugs-of-Abuse testing; for example, whether the sample is possibly diluted with water or other liquids as indicated by the creatinine and specific gravity tests. PrecisionDx detects whether the sample contains commercially available adulterants including nitrite, glutaraldehyde, bleach, pyridinium chlorochromate and other oxidizing agents. PrecisionDx can also assess whether the sample is possibly contaminated by acidic (vinegar) or basic (ammonia solution) adulterants as indicated by the pH test.
Our New No Flood Precision Multi Panel Drug Dip Test is a one-step urine test for simultaneous detection of drugs in urine. Custom configurations are available on all rapid drug test products. Features Ce Mark, Health Canada II & III Up to 99% accuracy, USA Made strips and reagents Immediate Rapid Results: Read Negatives within 1 minute, positives in 5 minutes Simple Dip & Read Easy to read strips with definitive lines 40+ Drug Test options No dip requirement can full immerse in urine without flooding 24 Month Shelf Life from Date of manufacture Results Remain Valid Up To 1 Hour OEM & Private Label available Call for volume discounts! Benefits Same Money & Quality Product Superior Personal Service Available after regular business hours Free Online Training, Product Certification, Product Training Video Free Lab LC-MS/MS set up, free overnight shipping, airbills, boxes, lab packs, specimen bags These are screening devices read positive or negative, qualitative, and although highly accurate, if you read a positive we recommend a certified lab for LC-MS/MS Confirmation. These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
CLIA Waived Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests. This test is also authorized for use with fingerstick whole blood specimens only at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation. The CLIA Waived COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only. Indication: Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized laboratories. About Test Device EUA Authorized CE Mark Test does NOT give positive or negative result for COVID-19 virus. This is an antibody test, it only indicates past or recent infection. Read Results in 15 Minutes 9 Month Expiration from Date of Manufacture Contents 20 Test Devices 20 Disposable Pipettes 20 Alcohol Prep Pads Sterile Safety Lancets Buffer Package Insert
Latex, non sterile, powdered and powder-free, textured fingertips Single-use, ambidextrous gloves made from narutal latex. Suitable for food handling, laboratory and industrial applications with complex risks and for medical applications. * Free from phthalates and softeners * Textured fingertips for excellent grip * Rolled cuffs minimise the risk of tearing * CE, FDA, EN 455, EN 374 * Food contact approved Disposable/Reusable Disposable Powdered/Powder-free Powder-free Finish Textured fingertips Cuff style Beaded Cuff thickness 0,16 mm* Finger thickness 0,22 mm* Palm thickness 0,20 mm* EN norm CE, FDA, EN 455, EN 374 size Unit of Sale Small Box 100 - 10 box/carton Medium Box 100 - 10 box/carton Large Box 100 - 10 box/carton Extra Large Box 100 - 10 box/carton
Nitrile, non sterile, powder-free, textured finish For laboratory use in pharmaceutical, industrial and medical applications and in the food industry. These ambidextrous gloves provide extra protection,particularly for sensitive skin. * Highly resistant to chemical solvents and fats * Excellent grip, especially when holding wet objects * Designed especially for latex allergy sufferers * CE, FDA, EN 455, EN 374 Food contact approved Disposable/Reusable Disposable Powdered/Powder-free Powder-free Cuff style Beaded Cuff thickness 0,20 mm* Finger thickness 0,30 mm* Palm thickness 0,22 mm* EN norm CE, FDA, EN 455, EN 374 Size Unit of Sale Small Box 100 - 10 box/carton Medium Box 100 - 10 box/carton Large Box 100 - 10 box/carton Extra Large Box 100 - 10 box/carton
Product Type: Gloves- Nitrile Exam Brand: Ansell Color: Blue Size: S, M, L, XL Quantity Per Package: 300 Nitrite Powder-Free Gloves are commonly used by medical and dental professionals, tattoo artists, spas and salons and in laboratory settings. Nitrite is waterproof, grease-proof, oil proof and most importantly, chemically resistant to a range of common chemicals and substances. Details: Material: Nitrite Grade: Medical Grade Examination 100% Latex Free and DEHP Free FDA Approved and CE Certified - ASTM D6319 Nitrite gloves are made with synthetic rubber that surpasses latex in every way: Higher puncture resistance Higher chemical/liquid/gas protection Heavy duty strength Higher tactile sensitivity without sacrificing any of the above
Patriot Mask Molded N95 Respirator - Small Key Features: Size: Small Meets NIOSH inhalation procedure testing TEB-APR STP 0007. 99 % BFE (Bacterial Filtration Efficiency) according to ASTM 99.7% Filter Efficiency according to ICS Laboratories Inc. Berry Amendment (10 U.S.C. 2533a) compliant. Pre-formed for secure fit and for easy breathing. Bendable nose clip will help provide custom fit and secure seal. Available in Small and Regular Latex free: Yes Model: Collapse Resistant Cup/Procedure (Surgical Pending) Material Composition: Outer Layer: Spun bound cloth/non woven fabric (Teal) Filter: Melt blown non woven fabric (2 layers) Inner Layer: Needle punch cotton Nose Clip: 1 mm thick metal Nose Foam: Spandex filament sponge bar Headband: Nylon
Fingertip textured | Tested for use with various lab chemicals and chemotherapy drugs1 | FLEXAL level protection | Standard protection within High Use portfolio | Available in premium packaging configuration- Flexal with dispensing film | Not made with natural rubber latex | Ambidextrous | Powder-free | Color: Cornflower blue | Nominal fingertip thickness: 3.7mil (.10mm) | USP compliant2 | Footnotes and references: | *GHX/ HPIS D_MAT2015 | 1 Caution: Gloves used for protection against chemotherapy drug and laboratory chemical exposure should be selected specifically for the type of chemicals being used. | 2This Cardinal Health product helps healthcare facilities comply with the USP standard for the safe handling of hazardous drugs. Note: Review Safety Data Sheets (SDS) for the chemicals/ drugs being used to determine required level of protection.
The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within the first five days of symptom onset or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet the requirements to perform moderate, high, or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., inpatient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation. Lateral flow assay Detect SARS-CoV-2 nucleocapsid protein antigen Rapid results within 10-15 minutes Intended at POC setting (i.e., in patient 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 nasopharyngeal swab 87.18% PPAa and 100% NPAb when used with anterior nasal swab
Precision - Saliva Scan - 10 Panel - THC/COC/AMP/OPI/mAMP/PCP/BAR/BZO/OXY/BUP Our New Precision Saliva Drug Test is an inexpensive screening test for the simultaneous detection of drugs in human saliva. Custom configurations are available on all rapid drug test products. Features CE Mark, Health Canada II & III 99% accuracy, USA Made strips and reagents Immediate Rapid Results: Read Negatives within 1 minute, positive in 5 minutes Simple Swab, insert, and read results Easy to read strips with definitive lines Swab stem color indicator ensures optimal saliva saturation/collected. 25+ Drug Test options 24 Month Shelf Life from Date of manufacture Results Stable for 30 Hour OEM & Private Label available Call for volume discounts! Benefits Same Money & Quality Product Superior Personal Service Available after regular business hours Free Online Training, Product Certification, Product Training Video Free Lab LC-MS/MS set up, free overnight shipping, air bills, boxes, lab packs, specimen bags These are screening devices read positive or negative, qualitative, and accurate, if you read positive, we recommend a certified lab for LC-MS/MS Confirmation. These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
The Precision Plus Multi Panel Dip Card offers a fast, easy, and accurate test for the detection of drugs in human urine. Our New Precision Multi Panel Drug Dip Card Test has no flood technology and is a one-step urine test for simultaneous detection of drugs in urine. Custom configurations are available on all rapid drug test products. Features Health Canada II & III Up to 99% accuracy, USA Made strips and reagents Immediate Rapid Results: Read Negatives within 1 minute, positives in 5 minutes Simple Dip & Read Easy to read strips with definitive lines 40+ Drug Test options No dip requirement can full immerse in urine without flooding 24 Month Shelf Life from Date of manufacture Results Remain Valid Up To 1 Hour OEM & Private Label available Call for volume discounts! Benefits Same Money & Quality Product Superior Personal Service Available after regular business hours Free Online Training, Product Certification, Product Training Video Free Lab LC-MS/MS set up, free overnight shipping, airbills, boxes, lab packs, specimen bags These are screening devices read positive or negative, qualitative, and although highly accurate, if you read a positive we recommend a certified lab for LC-MS/MS Confirmation. For more information dial 1-866-526-2873 or email sales@americanscreeningcorp.com. These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
Our New No Flood Precision Multi Panel Drug Dip Test is a one-step urine test for simultaneous detection of drugs in urine. Custom configurations are available on all rapid drug test products. Features Ce Mark, Health Canada II & III Up to 99% accuracy, USA Made strips and reagents Immediate Rapid Results: Read Negatives within 1 minute, positives in 5 minutes Simple Dip & Read Easy to read strips with definitive lines 40+ Drug Test options No dip requirement can full immerse in urine without flooding 24 Month Shelf Life from Date of manufacture Results Remain Valid Up To 1 Hour OEM & Private Label available Call for volume discounts! Benefits Same Money & Quality Product Superior Personal Service Available after regular business hours Free Online Training, Product Certification, Product Training Video Free Lab LC-MS/MS set up, free overnight shipping, airbills, boxes, lab packs, specimen bags These are screening devices read positive or negative, qualitative, and although highly accurate, if you read a positive we recommend a certified lab for LC-MS/MS Confirmation. For more information dial 1-866-526-2873 or email sales@americanscreeningcorp.com. These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
Our New Precision Multi Panel Drug Dip Card Test has no flood technology and is a one-step urine test for simultaneous detection of drugs in urine. Custom configurations are available on all rapid drug test products. Features Health Canada II & III Up to 99% accuracy, USA Made strips and reagents Immediate Rapid Results: Read Negatives within 1 minute, positives in 5 minutes Simple Dip & Read Easy to read strips with definitive lines 40+ Drug Test options No dip requirement can full immerse in urine without flooding 24 Month Shelf Life from Date of manufacture Results Remain Valid Up To 1 Hour OEM & Private Label available Call for volume discounts! Benefits Same Money & Quality Product Superior Personal Service Available after regular business hours Free Online Training, Product Certification, Product Training Video Free Lab LC-MS/MS set up, free overnight shipping, airbills, boxes, lab packs, specimen bags These are screening devices read positive or negative, qualitative, and although highly accurate, if you read a positive we recommend a certified lab for LC-MS/MS Confirmation. For more information dial 1-866-526-2873 or email sales@americanscreeningcorp.com. These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
Disposable Or Non- Disposable(Textile) - Sms Disposable On Ecomm Site (Ship To Houston) - Yes Items Included - Level 2 - 1 Pc Straight Type Surgical Insulation Gown - Non Sterile Description - "Straight Type Surgical Insulation Gowns, Long Below The Knees, Crossed On The Back Neck Round With Adjustable Cuffs, Waterproof To The Penetration Of Liquids And Fluids, Anti-static And Resistant To Tension. Non Sterile And Disposable. Made With Fabric Made From 100% Antibacterial 35 Gsm Polypropylene Sms, Double Fabric At Front And Arms Level 2 For Use In Intensive Care Unit And Pathology Laboratory" Size - M / L / Xl Factory Exworks Price (Puebla Mexico) Us$ Dollars - $ 1.51 Ex Works Cost Per Case - $ 105.70 W/udi Fda Barcode Cost Per Label - $ 0.30 Factory Exworks Price (Puebla Mexico) Us$ Dollars W/udi Fda Barcode - $ 1.52 Ex Works Cost Per Case W/udi Fda Barcode - $ 106.00 Landed Us Warehouse Cost (+10%) - $ 1.67 Units Per Case - 70.00 Cases Per Pallet - 25.00 Number Of Pallets - 8.00 Total Cases - 200.00 Total Units To Be Shipped - 14,000.00 Total Value Shipped - $ 21,140.00 Total Value In Warehouse - $ 23,408.00
