abbott id now competency assessment10 marca 2023
abbott id now competency assessment

We have remained at the forefront of medicine by fostering a culture of collaboration, pushing the boundaries of medical research, educating the brightest medical minds and maintaining an unwavering commitment to the diverse communities we serve. EUA supports flexible near patient testing environments. c. Send the completed POC Corrected Report Form to the lab. 178 0 obj <>/Filter/FlateDecode/ID[<301DDEECFAA1D3498BAA66861BB1A194><151D3900F17130438FFBD093DE37C0D5>]/Index[158 36]/Info 157 0 R/Length 101/Prev 91471/Root 159 0 R/Size 194/Type/XRef/W[1 3 1]>>stream ! There are templatesin the, Competency frequency: Initial training, 6-months, and annually thereafter. 1. Here are the instructions how to enable JavaScript in your web browser, One Abbott solution for patient testing, result capture and data reporting, Isolation Precautions in Healthcare Settings, Emergency Use Authorization of Medical Products and Related Authorities. i-STAT Operator Training Checklist i -STAT Competency Assessment 6-Month/Annual i-STAT Competency Written Test i-STAT INR Finger stick Training and Assessment Record i-STAT Cartridge Room Temperature Log i-STAT Corrective Action Log i-STAT Record of Receipt/QC Log HemoCue Hemoglobin Procedure HemoCue Hemoglobin Job Aid HemoCue Training Checklist 1 0 obj The portable, rapid molecular ID NOW COVID-19 test has emerged as a critical part of this arsenal, allowing fast diagnosis with results in 13 minutes or less in a variety of locations such as physicians' offices, urgent care clinics and other point-of-care locations. They have higher throughput ID NOW delivers results in minutes where they're needed most during COVID-19. Learn how to use the test by watching the COVID-19 demonstration video. Learn all about the ID NOW Instrument and installation by following these video modules. Here are the instructions how to enable JavaScript in your web browser. Not all products are available in all regions. A Leader in Rapid Point-of-Care Diagnostics. Your use of this website and the information contained herein is subject to our Website Terms and Conditions and Privacy Policy: US Citizens | Non-US Citizens. hb``b``101G3020cdeY99E)3~H310pf ce`LqX` ! Perform the testing using all 9's as the patient ID. hZmo7+xE,_4m ,_;#TG@Vpy P%3+dRX'01PiB#BL HP1J%fBQ(C%KBA)P)A ID NOW PERFORMANCE, FROM RESEARCHERS IN THE FIELD Reliable test results depend on many factors, conformity to test design. DIFFERENCE-MAKING INNOVATION. Facility-based platforms . All rights reserved. Do not remove swab. Abbott requires new usersto perform 1 positive and 1 negative/blank test controls prior to testing. The website that you have requested also may not be optimized for your screen size. endobj No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. hb```b``Vb`e``fd@ A+&fZlU7. As long as the barcode on the ID band scans, it is acceptable to use for testing. <8uFy6]Z+4\``wty/YPXQ.Fy5*Wv=?iC{u^nje(}a,_oMp1=;g=P#g|NerC?[=[2UraNy6?S\0CI~'+xMy5 COVID-19 RAPID TESTS: READY WHEN EVERY MINUTE COUNTS. 4485 0 obj <> endobj %PDF-1.6 % 193 0 obj <>stream If your non-waived laboratory is . Not all products are available in all regions. The ID NOW COVID-19 assay is now available for use on the ID NOW platform under U.S. Food and Drug Administration Emergency Use Authorization (EUA). This test is to be performed only using respiratory specimens collected from individuals who are . 112 No. Reliable test results depend on many factors, conformity to test design. endstream endobj startxref This website is governed by applicable U.S. laws and governmental regulations. A Leader in Rapid Point-of-Care Diagnostics. Your employee ID number, which can be scanned into the meter using the barcode on your ID badge. POC Maintenance Record : 2/13/2023: POC Regional Health Centers and Tests Chart. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Insert the (+) or (-) control swab into BOTTOM HOLE and firmly push upwards so that the swab tip is visible in the TOP HOLE. Abbott Diagnostics Scarborough, Inc. - ID NOW COVID-19. 158 0 obj <> endobj ID NOW IS A COMPLETE GAME-CHANGER FOR TESTING. At remote locations, testing is done using an ID NOW analyzer 2. POC:Piccolo Electrolyte Panel Reagent/QC Log: . For in vitro diagnostic use only. ! GoHealth Urgent Care: Rapid test kept COVID-19 patient from boarding plane. ^ ` r ` r O ! Explore fellowships, residencies, internships and other educational opportunities. The ID NOW test has emerged as a critical part of the fight against COVID-19, allowing fast diagnosis with results in minutes. 1. We are committed to providing expert caresafely and effectively. Each Abbott ID NOW COVID-19 test cartridge comes with a swab and all the necessary reagents. 4 0 obj Cholestech LDX Analyzer. The ID NOW platform combines the benefits of speed and accuracy for the fastest molecular results in the market. stream COVID-19 Product Insert. Sites would need to ensure the following steps are completed prior to use of the Abbott ID NOW analyzer for patient testing of COVID-19: For diagnostic testing of specimens conducted outside of a BSL-2 laboratory, such as rapid respiratory testing performed at the point of care, use Standard Precautions to provide a barrier between the specimen and personnel during specimen manipulation. SOP for Abbott ID NOW COVID-19 Point of Care Testing. b. 2 0 obj endstream endobj 159 0 obj <. 3 0 obj The ID NOW COVID-19 rapid test delivers high-quality molecular positive results in as little as 5 minutes, targeting the coronavirus (COVID-19) RdRp Gene. %PDF-1.5 % How advanced molecular testing technology detects novel coronavirus. Title: Abbott ID Now Competency Assessment Effective date: 29/10/2022 Author: A. Bromley Checked by: M. Ribeiro Approved by: M. Ribeiro Page 1 of 1 Title: COPY At Physician's Immediate Care, same high confidence in accuracy of results. Reporting of results (per Abbott Instructions for Use) should include: Reporting of false-positives and false-negatives and other significant deviations from performance characteristics to Abbott and FDA. <>/XObject<>/Font<>/ProcSet[/PDF/Text/ImageB/ImageC/ImageI] >>/MediaBox[ 0 0 720 540] /Contents 4 0 R/Group<>/Tabs/S/StructParents 0>> Check with your local representative for availability in specific markets. Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. Our unique ID NOW isothermal nucleic acid amplification technology provides molecular results in just minutes, allowing you to make effective clinical decisions sooner. Testing location should be reviewed to ensure minimal traffic for testing location, separate room if possible, location should be near asink and eyewashstation. Copyright 2007-2023. Based on your current location, the content on this page may not be relevant for your country. At Physicians Immediate Care, ID NOW helps them slow the spread of COVID-19. endstream endobj startxref ID NOW is a leading molecular point-of-care platform in the United States, trusted by hospitals, physician offices, and urgent care clinics nationwide. For in vitro diagnostic use only. Learn about career opportunities, search for positions and apply for a job. ID NOW COVID-19 and ID NOW COVID-19 2.0 have not been FDA cleared or approved. Sign up to receive valuable updates from Abbott. Rotate (twirl) swab shaft 3 times CLOCKWISE (to the right). ID NOW COVID-19 2.0. The purpose of the study is to evaluate the clinical sensitivity of buccal swab testing using Abbott ID NOW COVID-19device to detect SARS-CoV-2 infection among children aged 0-<18.0 years old presenting to the emergency department with an indication for SARS-CoV-2 testing as . %PDF-1.5 Abbott's approach to research and development of COVID-19 diagnostic tests. Template log sheetscan be found under the Abbott IFU, Test Product Insert, CLSI folder >, Training of all users on the Abbott ID NOW analyzer using the 8 modules provided by Abbott, Competency of individuals need to be assessed using the appropriate requirements per your CLIA certificate, accrediting organizational requirements and/or local policyrequirements. Photos displayed are for illustrative purposes only. Afinion 2. i-STAT 1 Wireless. For more information about these cookies and the data Find out more about this innovative technology and its impact here. The products and information contained herewith may not be accessible in all countries, and Abbott takes no responsibility for such information which may not comply with local country legal process, regulation, registration and usage. Running a Patient Test. (2003) Impact of the Rapid Diagnosis of Influenza on Physician Decision-Making and Patient Management in the Pediatric Emergency Department: Results of a Randomized, Prospective, Controlled Trial. endobj Abbott ID Now Covid19 QC & Patient Results Log Negative Ok Barcode Negative Barcode Negative Alternatively, click YES to acknowledge and proceed. We use cookies and other tools to enhance your experience on our website and Bonner, A.B. Why is it important to make sure the patient ID band is replaced when a patient is transferred in from other facility? The instrument then amplifies the virus hundreds of millions of times to make it more easily detectable and determine at a molecular level whether the sample is positive or negative. Links which take you out of Abbott worldwide websites are not under the control of Abbott, and Abbott is not responsible for the contents of any such site or any further links from such site. Documentation of maintenance and temperature should be included in the SOP. endstream endobj 4486 0 obj <>/Metadata 132 0 R/Outlines 299 0 R/PageLayout/OneColumn/Pages 4479 0 R/StructTreeRoot 362 0 R/Type/Catalog>> endobj 4487 0 obj <>/ExtGState<>/Font<>/XObject<>>>/Rotate 0/StructParents 0/Tabs/S/Type/Page>> endobj 4488 0 obj <>stream NcTSpooR,l3 and the IQCP must contain the three required elements (Risk Assessment, Quality Control Plan, and . Properly used, ID NOW very effective, Abbotts John R. Hackett Jr. tells CNN. _____The patient test result displays 423mg/dl. POC I-STAT Training/Competency Checklist: 4/15/2021: POC Bassett Clinics and Tests Chart. This study will enroll approx 2882 participants under the age of 18 at 15 pediatric emergency centres across Canada. Updated as of 12/08/2022 . hbbd```b``y"gH sd`Wu0y LnOYc $FZ ' H (bt{ I Risk Assessment. US Centers for Disease Control (CDC) Coronavirus (COVID-19) Webpages Let us help you navigate your in-person or virtual visit to Mass General. Signed Competency Checklist should be maintained in employee's personnel file (see Nasal Swabbing Procedure and Performance of BinaxNOWTM COVID-19 Ag Card Competency Checklist) It is greater than 423. . PPE training 6. Close and securely seal the card. Learn how Abbott utilizes unique isothermal nucleic acid amplification technology. <> Creation of SOP for COVID-19 testingusing the Abbott ID NOW analyzer. Pediatrics Vol. 884 0 obj <>stream CONDUCTING RESEARCH DURING THE COVID-19 PANDEMIC. Abbott ID Now - Training/Orientation Trainee: Date of Training: Test Name: COVID-19/SARS CoV-2 : Trainer: This document is used to verify that the Trainee responsible for running the COVD-19 test has reviewed the Online Training modules and received sufficient training to include the following: collected, please refer to our Privacy Policy. 21. %PDF-1.5 % ID NOW: THE FOREFRONT OF COVID-19 TESTING. Any person depicted in such photographs is a model. The ID NOW COVID-19 assay is now available for use on the ID NOW platform under U.S. Food and Drug Administration Emergency Use Authorization (EUA). The products and information contained herewith may not be accessible in all countries, and Abbott takes no responsibility for such information which may not comply with local country legal process, regulation, registration and usage. <>>> %%EOF The device is connected to a CONNECT Universal Gateway using an ethernet cable 3. Procedure Specimen Collector Competencies Specimen Collectors are required to complete the following competencies to ensure they have a basic understating of the Abbott Binax Nowtm COVID-19 test: 1. a. It is a high critical result. The Point of Care Testing Procedure Manual contains the approved procedures for safe and effective operation of POCT procedures by MGH POCT providers. q.UV+Soeo6[\}J'.p&LuJ-wZeo,;?7*Z@AUP }43*!4 yBH &3LVnu"M%A`I$X4 M%!J'r-YZdiI3e,9Y:3tf3Cg #`d0FH02 F#H$8, K#H$8, @g,9:$@tL33GgBg#`1. SOP/POCT/69/2 hbbd```b``+A$S+p=d`LN @E0 D2&$cV"sB#ZKGI:G0 {+ Your Social Security Number c. All 9's (99999999) This test has not been FDA cleared or approved. b. Competency Sheet. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product . Complete the ID NOW Assessment Form, Maintain competency on the Abbott ID NOW POCT COVID-19 test system, Follow accreditation requirements for patient identification, testing and reporting. How TO USE SOLUTION If surfaces are dirty, they should first be cleaned with detergent or soap and waterprior to disinfection with HALT solution. Abbott - A Leader in Rapid Point-of-Care Diagnostics. ID NOW Molecular Technology Overview Animation Global (English), California Transparency in Supply Chains Act, Declaration for California Compliance Law, instructions how to enable JavaScript in your web browser, Easy to use with only minimal training requirements, Large visual touchscreen displays results, eliminating transcription errors and the need for printing, Small footprint saves you bench space and can be used in any healthcare setting, Eliminates interpretation and transcription errors, Gives you the confidence to make clinical decisions sooner, Enables prompt initiation of infection control measures, Aids targeted antiviral therapy and Antimicrobial Stewardship, Reliable near-patient testing reduces overall healthcare costs. Check with your local representative for availability in specific markets. ! Wxyh[} P"%"l0T( For American Family Care, ID NOW is vital tool to helping its community. SIZE OF A TOASTER. 4577 0 obj <>stream The intuitively designed ID NOW instrument can have a positive impact in any healthcare setting. Contact Sales Technical Support Overview Benefits Helpful Documents lcKjs.&g$=HP^CGB*oWSXu4V?Tjilp?yTT)#JL-dyB~&%fomy:qIJ. CONDUCTING RESEARCH DURING THE COVID-19 PANDEMIC 2023 Abbott. G D J r 0~0 b ^ H &. Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. 10/19/2020. endstream endobj startxref REDUCING RISK BY DIAGNOSING WITH RELIABLE RAPID TEST ID NOW delivers results in minutes where they're needed most during COVID-19. OVERVIEW; FINANCIALS; STOCK INFO; . Abbott - A Leader in Rapid Point-of-Care Diagnostics. The tests have been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens, and are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. The SOP should encompass information pertaining to instructions for reporting and documenting results, notification of positive results, appropriate PPE usage and cleaning procedures, quality control, etc. The SOP should encompass information pertaining to instructions for reporting anddocumentingresults, notification ofpositive results,appropriate PPE usage andcleaning procedures, quality control, etc. Specimen Collection, World Health Organization (WHO) Coronavirus (COVID-19), U.S. Food & Drug Administration BinaxNOW COVID-19 . The General Hospital Corporation. For full functionality of this site it is necessary to enable JavaScript. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Search for condition information or for a specific treatment program. Please review our privacy policy and terms & conditions. GDPR Statement (last updated: May 2018) | California Transparency in Supply Chains Act | Declaration for California Compliance Law. %%EOF Sign up to receive valuable updates from Abbott. ID NOWis a rapid, instrument-based, isothermal system for the qualitative detection of infectious diseases. For i-STAT test cartridge information and intended use, refer to individual product pages or the cartridge information (CTI/IFU) in the i-STAT Support area. Please be aware that the website you have requested is intended for the residents of a particular country or region, as noted on that site. This website is governed by applicable U.S. laws and governmental regulations. The ID NOW COVID-19 test returns positive results in 13 minutes or less to enable immediate clinical decisions during the first patient visit. Title (Mr/Mrs/Miss/Dr): Surname: Position: Forename(s): . BinaxNOW Influenza A&B Card 2. For full functionality of this site it is necessary to enable JavaScript. endobj REDUCING RISK BY DIAGNOSING WITH RELIABLE RAPID TEST. Watch the replay for multi-disciplinary updates on variant surveillance and testing protocols from Europe to the U.S., and explore COVID-19 testing protocols to optimize patient care and public health readiness with an uncertain upcoming influenza season. (BLUE) and G3+ (BLUE) are now considered high complexity tests due to lack of FDA categorization. Notification to CMS and yourclinic accrediting organizationof intent to perform COVID-19 testing using the Abbott ID NOW analyzer under the FDA EUA for COVID-19. Preform a Quality Control Test and/or patient test on self/coworker with Super User Supervision 8. Please see ID NOW Instrument User manual for additional operating environment requirements. hbbd```b``Z"Ig6D&Hw0LH40{7U W ;|zFg`` {yJ Information for Laboratories Competency must be verified by competent trainer, by performing the testing procedure outlined by Abbott. ID NOW is significantly faster than other molecular methods and more accurate than conventional rapid tests. Safe Care CommitmentGet the latest news on COVID-19, the vaccine and care at Mass General.Learn more. ID NOW PERFORMANCE, FROM RESEARCHERS IN THE FIELD. % 798 0 obj <> endobj 4507 0 obj <>/Filter/FlateDecode/ID[<38B5EDDB3DE12F4286DDB68BF53A81A2><158FB707B081FF49B9233C9305EF120D>]/Index[4485 93]/Info 4484 0 R/Length 111/Prev 437721/Root 4486 0 R/Size 4578/Type/XRef/W[1 3 1]>>stream Our uniqueID NOWisothermal nucleic acid amplification technology provides molecular results in just minutes, allowing you to make effective clinical decisions sooner. Apply HALT solution to hard, non-porous surfaces. Instrument User Manual. 0 In the context of an evolving digitally-oriented library and/or information science (LIS) discipline and framed by Andrew Abbott's Chaos of Disciplines theory, this article presents an epistemological overview of evolving competency requirements for a global digital information environment and the implications of this for future LIS education. O ! The website you have requested also may not be optimized for your specific screen size. All rights reserved. What does this mean? POC Abbott ID Now QC Log: 2/18/2021: POC HemoCue Hgb QC Log (Form will be sent by POC with QC Material.) <> 2/27/2020. Laboratory Biosafety Positive and Negative Control Swabs. This test has been authorized by FDA under an EUA for use by authorized laboratories. Influenza A & B Package Insert. As a result, the site may contain information on pharmaceuticals, medical devices and other products or uses of those products that are not approved in other countries or regions. SoToxa Mobile Test System. ID NOW Ellution Buffer. 821 0 obj <>/Filter/FlateDecode/ID[<328C757F408E7C41BFC7E242F2973DD0>]/Index[798 87]/Info 797 0 R/Length 112/Prev 216100/Root 799 0 R/Size 885/Type/XRef/W[1 3 1]>>stream 0 Gateway transmits test data via secure cellular connectivity to a secure Abbott-hosted, cloud-based server 4. Learn all about the ID NOW Instrument and installation by following these video modules. General Coronavirus (COVID-19) Alternatively, click YES to acknowledge and proceed. For i-STAT test cartridge information and intended use, refer to individual product pages or the cartridge information (CTI/IFU) in the i-STAT Support area. Enter your email address to receive Abbott Edge. Determine HIV-1/2 Ag/Ab Combo. All surfaces must REMAIN WET FOR 10 MINUTES for maximum disinfection. FAQ # Description of Change . Learn about the many ways you can get involved and support Mass General. ID NOW uses a liquid solution designed to deactivate the virus and break it apart to expose the RNA. 0 Learn how to use the Strep A 2 test by watching this product demonstration. PORTABLE, RELIABLE AND RAPID, WITH RESULTS ON THE SPOT, ALL IN THE ID NOW is a leading molecular point-of-care platform in the United States, trusted by hospitals, physician offices, and urgent care clinics nationwide. At Mass General, the brightest minds in medicine collaborate on behalf of our patients to bridge innovation science with state-of-the-art clinical medicine. Specimen handling and collection training 7. b. Larger POC platforms, such as the Cepheid GeneXpert Xpress, another example of a POC device that can be used for COVID -19, are often based in hospitals and medical centers. RXqGfhdP)bkfhp.F!0!\ % d,W+EB9,g053051%2973b[2 wg Hi@ (n@Z(13~?V@1& Any person depicted in such photographs is a model. MoreCDC guidelinesfor COVID-19 can be found using the following links. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. Z{sB[u.j(t\G#Hu F+Aal+ 5N# J FzPxT, JdA5dr.u+%c6l+"jQP) #u(FJ #uVDHi"zDLQyhE.3 &ztxFJ)1`l5td#z$ z%HJG R{8djdlRg U]S[W_PX"YHE.ud]$"YH6E)MldS$"gdF3\|NMVEw^:&V?jr+8^"MB"r;*i(. 2. The ID NOW COVID-19 assay is a qualitative, rapid molecular test that utilizes an isothermal nucleic acid amplification technology to detect nucleic acid from the SARS-CoV-2 viral RNA. RAPID TESTING CAN GET PEOPLE THE RIGHT TREATMENT. They have been authorized by the FDA under an emergency use authorization for use by authorized laboratories. Learn about simple, reliable and secure connectivity and reporting for ID NOW COVID-19 testing. For procedures with a high likelihood to generate aerosols or droplets, use either a certified Class II Biological Safety Cabinet (BSC)oradditional precautions to provide a barrier between the specimen and personnel. Point-of-care tests are critical to help fight the novel coronavirus pandemic. Intended for U.S. residents only. b. Frequently Asked Questions (FAQs), Abbott i- STAT . hb```b``Ve`e``efd@ A+E- Peel off adhesive liner from the right edge of the test card. Anesthesia, Critical Care & Pain Medicine, Billing, Insurance & Financial Assistance, Room Temperature Monitoring Information and Log sheet, Clinitek Status Training and Competency Assessment, Visual Dipstick Training & CompetencyAssessment, Outpatient (all others) Urine QC Log Sheet, Urine HCG PregnancyTraining & Competency, -STAT Competency Assessment 6-Month/Annual, i-STAT INR Finger stick Training and Assessment Record, HemoCue Docking Station and QC Guidelines, Rapid Strep Training & Competency Assessment, DCA Vantage Maintenance Job Aid (Procedure), DCA Vantage HgbA1C Training & Competency Assessment, DCA Vantage Optical Test Cartridge Result Log, ACT Competency Assessment 6-month/AnnualDocumentation tool, ACT Training & Competency Quiz/ObservationTool-Annual, AVOXimeter Initial Training & Assessment Record, AVOXimeter 6 month and Annual Competency Documentation, Modified GC Screen 6 month and Annual Competency Documentation, Modified GC Screen Quiz and Observation Checklist, Modified GC Screen Alternate Proficiency Result Form, GEM 5000 Competency Documentation-6 month and annual POCT, GEM 5000 Operator Training Checklist POCT, CoaguChek XS Initial Learning and Training Assessment, PPM Competency Assessment Completion Guideline, Quality Control - Reagent Storage, Ordering and Documentation Guide, Joint Commission Preparation Checklist for POCT Site Coordinators. Please click NO to return to the homepage. Competency Exam Initial Competency Semi-annual Competency Annual Competency (CY: _____) Follow up This exam is to be performed upon Initial Orientation & Training and Competency; twice in the first year of practice; and annually thereafter. Isolation Precautions in Healthcare Settings Abbott is providing these links to you only as a convenience, and the inclusion of any link does not imply endorsement of the linked site by Abbott. *For Product Labeling documents, such as the Package Insert, Quick Reference Guide, SDS sheets and CLSI documents, please visit our e-IFU website. COVID-19 Transport Tube Product Sheet (English), Cross Division COVID-19 Variant Technical Brief NORAM (English), ID NOW COVID-19 CLSI + More Packet (English), ID NOW COVID-19 Elution Buffer SDS (English), ID NOW COVID-19 Nasal Swab Collection Technical Tips (English), ID NOW COVID-19 Nasopharyngeal Swab Collection Technical Tips (English), ID NOW COVID-19 One Abbott Solution Brochure (English), ID NOW COVID-19 Procedural Control Results and Patient Record (English), ID NOW COVID-19 Procedural Control Results and Patient Record Word (English), ID NOW COVID-19 Product Sheet US (English), ID NOW COVID-19 Throat Swab Collection Technical Tips (English), ID NOW Positive and Negative Control Swabs SDS (English), Technical Brief Current COVID-19 Vaccinations and Detection by Abbott BinaxNOW COVID-19 Ag Card and ID NOW COVID-19 2.0 Assay September 2022 (English), California Transparency in Supply Chains Act, Declaration for California Compliance Law, instructions how to enable JavaScript in your web browser, ID NOW COVID-19 Control Kit (12 pos, 12 neg), Positive results may be detected in as little as 5 minutes, Molecular technology targeting COVID-19 RdRp gene, Designed for near patient testing in a variety of healthcare environments, Direct sample types include: Nasal, Throat, and Nasopharyngeal swabs, Small footprint enables ease of use at point of care, Dimensions - 8.15 W x 5.71 H x 7.64 D (207 mm W x 145 mm H x 194 mm D), Assay kit contains all necessary components for testing to include: 24 tests, swabs for sample collection, pipettes, positive and negative controls.

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