Other products from "TELEFLEX INCORPORATED"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00816000011942 IPN033711 9001-VC-005 EZ-IO(R) 25mm Needle Set FMI Needle, hypodermic, single lumen 2 ARROW
2 00816000012284 IPN033813 9468-VC-006 OnControl(R) Aspiration System Needle Set, 68mm FCG Biopsy needle 2 ARROW
3 00816000012277 IPN033817 9490-VC-006 OnControl(R) Aspiration System Needle Set, 90mm FCG Biopsy needle 2 ARROW
4 00816000011980 IPN033767 9079-VC-005 EZ-IO® 45mm Needle Set FMI Needle, hypodermic, single lumen ARROW
5 00816000011973 IPN033766 9079-VC-001 EZ-IO(R) 45mm Needle Set FMI Needle, hypodermic, single lumen 2 ARROW
6 00816000011966 IPN033729 9018-VC-005 EZ-IO(R) 15mm Needle Set FMI Needle, hypodermic, single lumen 2 ARROW
7 00816000011959 IPN033728 9018-VC-001 EZ-IO(R) 15mm Needle Set FMI Needle, hypodermic, single lumen 2 ARROW
8 00816000011935 IPN033710 9001-VC-001 EZ-IO(R) 25mm Needle Set FMI Needle, hypodermic, single lumen ARROW
9 00816000011904 IPN033764 9079P-VC-005 EZ-IO® 45mm Needle + Stabilizer Kit FMI Needle, hypodermic, single lumen 2 ARROW
10 00816000011898 IPN033726 9018P-VC-005 EZ-IO® 15mm Needle + Stabilizer Kit FMI Needle, hypodermic, single lumen ARROW
11 00816000011881 IPN033708 9001P-VC-005 EZ-IO® 25mm Needle + Stabilizer Kit FMI Needle, hypodermic, single lumen 2 ARROW
12 00801902172662 IPN915878 IAH-09145 Disposable Helium Tank Adaptor DSP System, balloon, intra-aortic and control 2 ARROW
13 00801902172617 IPN915872 IAA-14695 AC3 AUSTRALIAN POWER CORD (16FT/5M) DSP System, balloon, intra-aortic and control 2 ARROW
14 00801902172600 IPN915870 IAA-14660 AC3 N. AMERICAN POWER CORD (13FT/4M) DSP System, balloon, intra-aortic and control 2 ARROW
15 00801902172556 IPN915865 IAA-03720 Phono to Mini Connector DSP System, balloon, intra-aortic and control 2 ARROW
16 00801902172495 IPN915863 IAA-03712 Slave Cbl-Phone to Phone Cbl Space Lab DSP System, balloon, intra-aortic and control 2 ARROW
17 00801902172457 IPN915858 IAA-00501 Slv Cbl-Phn to Phn Cbl Siemens Mod 9000 DSP System, balloon, intra-aortic and control 2 ARROW
18 00801902172402 IPN915855 IAA-00437E 5 LEAD ECG CABLE ASSEMBLY IEC DSP System, balloon, intra-aortic and control 2 ARROW
19 00801902172396 IPN915854 IAA-00437 5 LEAD ECG CABLE ASSEMBLY AHA DSP System, balloon, intra-aortic and control 2 ARROW
20 00801902172372 IPN915852 IAA-00402 Gould Xducer Adapter Cable DSP System, balloon, intra-aortic and control 2 ARROW
21 00801902172341 IPN915849 IAA-00175 IV POLE DSP System, balloon, intra-aortic and control 2 ARROW
22 00801902172297 IPN915844 IAA-00003 Slave Cable-Phone to Phone Cable For use with IABP DSP System, balloon, intra-aortic and control 2 ARROW
23 00801902136749 IPN038076 IAB-S730C Intra-Aortic Balloon: 7 Fr. 30 cc DSP System, balloon, intra-aortic and control 2 ARROW
24 00801902136732 IPN038077 IAB-S840C Intra-Aortic Balloon: 8 Fr. 40 cc DSP System, balloon, intra-aortic and control 2 ARROW
25 00801902136725 IPN038101 IAB-05830-LWS IAB: 8 Fr. - 30 cc DSP System, balloon, intra-aortic and control 2 ARROW
26 00801902136718 IPN038102 IAB-05840-LWS IAB: 8 Fr. - 40 cc DSP System, balloon, intra-aortic and control 2 ARROW
27 00801902136701 IPN038074 IAB-06830-U IAB: 7.5 Fr. - 30 cc DSP System, balloon, intra-aortic and control 2 ARROW
28 00801902136695 IPN038075 IAB-06840-U IAB: 7.5 Fr. - 40 cc DSP System, balloon, intra-aortic and control 2 ARROW
29 00801902111548 IPN036060 ASK-04001-DU5S1 Arrow(R) Access Kit for use with 5 Fr. Peripherally Inserted Central Venous Catheter LJS Catheter,intravascular,therapeutic,long-term greater than 30 days 2 ARROW
30 00801902111531 IPN036059 ASK-04001-DU4S1 Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter DYB INTRODUCER, CATHETER 2 ARROW
31 00801902111524 IPN036058 ASK-42703-PUHC Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 ARROW
32 00801902111470 IPN036055 ASK-04001-DU10 Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Veno Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter OBJ Catheter, ultrasound, intravascular 2 ARROW
33 00801902111463 IPN036054 ASK-04001-DU9 Arrow(R) VPS(R) Access Kit for use with 5 Fr. Peripherally Inserted Central Veno Arrow(R) VPS(R) Access Kit for use with 5 Fr. Peripherally Inserted Central Venous Catheter OBJ Catheter, ultrasound, intravascular 2 ARROW
34 00801902111456 IPN036053 ASK-45552-RWJ4 Arrowg+ard Blue Advance(TM) PICC Kit LJS Catheter,intravascular,therapeutic,long-term greater than 30 days 2 ARROW
35 00801902111449 IPN036052 ASK-45541-RWJ4 Arrowg+ard Blue Advance(TM) PICC Kit LJS Catheter,intravascular,therapeutic,long-term greater than 30 days 2 ARROW
36 00801902111432 IPN032636 AK-09001 Peritoneal Lavage Kit GBW CATHETER, PERITONEAL 1 ARROW
37 00801902111425 IPN032668 ASK-00001-1A Maximal Barrier Drape FYA GOWN, SURGICAL 2 ARROW
38 00801902111401 IPN030126 CS-22854-E Arrow-Howes(TM) Quad-Lumen Central Venous Catheterization Set with Blue FlexTip( Arrow-Howes(TM) Quad-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 ARROW
39 00801902111364 IPN036048 ASK-21242-UU3 Arrowg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7.5 Arrowg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters DYB INTRODUCER, CATHETER 2 ARROW
40 00801902111333 IPN036049 ASK-45703-PCC1 Pressure Injectable ARROWg+ard Blue Plus(R) Multi-Lumen Central Venous Catheterization Kit FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 ARROW
41 00801902111326 IPN036062 ASK-04100-CC Arterial Catheterization Kit DQX WIRE, GUIDE, CATHETER 2 ARROW
42 00801902111319 IPN034320 ASK-04120-CC Radial Artery Catheterization Kit DQX WIRE, GUIDE, CATHETER 2 ARROW
43 00801902111302 IPN034235 ASK-04018-CC Arterial Catheterization Kit DQX WIRE, GUIDE, CATHETER 2 ARROW
44 00801902109590 IPN036381 ASK-42703-PMSG Pressure Injectable ARROWg+ard Blue Plus(R) Multi-Lumen Central Venous Catheterization Kit FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 ARROW
45 00801902109583 IPN036379 ASK-45703-PMSG Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 ARROW
46 00801902109576 IPN035035 ASK-42854-PMSK1 Pressure Injectable ARROWg+ard Blue PLUS(R) Quad-Lumen Central Venous Catheterization Kit FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 ARROW
47 00801902105165 IPN030835 CV-04301 Central Venous Catheterization Set with Blue FlexTip(R) Catheter DQY CATHETER, PERCUTANEOUS 2 ARROW
48 00801902109552 IPN033066 CS-15422-SFX NextStep(R) Antegrade Hemodialysis Catheterization Set Long-Term Access. Cathete NextStep(R) Antegrade Hemodialysis Catheterization Set Long-Term Access. Catheter Length, Tip to Cuff: 42 cm MSD Catheter, hemodialysis, implanted ARROW
49 00801902109545 IPN033058 CS-15362-I Edge(R) Hemodialysis Catheterization Set Long-Term Access Catheter Length, Cuff Edge(R) Hemodialysis Catheterization Set Long-Term Access Catheter Length, Cuff to Tip: 31 cm MSD Catheter, hemodialysis, implanted 2 ARROW
50 00801902109538 IPN036396 ASK-04001-UH Spring Wire Guide Kit DQY CATHETER, PERCUTANEOUS 2 ARROW
Other products with the same Product Code "CAF"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00884389106894 HCSMONKEY HCSMONKEY COMPRESSOR,NEBULIZER, CHARACTER, MONKEY MEDLINE INDUSTRIES, INC. MEDLINE INDUSTRIES, INC.
2 00884389106870 HCS70004 HCS70004 COMPRESSOR,NEBULIZER,AEROMIST COMPACT Medline MEDLINE INDUSTRIES, INC.
3 00872237005093 63-515 NEBULIZER SET, ADULT (CONTAINS: ADULT ELONGATED MASK, NEBULIZER BOTTLE 6ML, 7' O NEBULIZER SET, ADULT (CONTAINS: ADULT ELONGATED MASK, NEBULIZER BOTTLE 6ML, 7' OXYGEN TUBE W/ STANDARD-UNIVERSAL CONNECTORS) GLOBAL HEALTHCARE GHC HEALTHCARE, INC.
4 00872237004850 63-565 NEBULIZER SET, PEDIATRIC (CONTAINS: PEDIATRIC ELONGATED MASK, NEBULIZER BOTTLE 6 NEBULIZER SET, PEDIATRIC (CONTAINS: PEDIATRIC ELONGATED MASK, NEBULIZER BOTTLE 6ML, 7' OXYGEN TUBE W/ STANDARD-UNIVERSAL CONNECTORS) GLOBAL HEALTHCARE GHC HEALTHCARE, INC.
5 00872237004836 63-560 NEBULIZER SET, PEDIATRIC (CONTAINS: PEDIATRIC ELONGATED MASK, NEBULIZER BOTTLE 6 NEBULIZER SET, PEDIATRIC (CONTAINS: PEDIATRIC ELONGATED MASK, NEBULIZER BOTTLE 6ML, 7' OXYGEN TUBE W/ STANDARD-STANDARD CONNECTORS) GLOBAL HEALTHCARE GHC HEALTHCARE, INC.
6 00872237004829 63-510 NEBULIZER SET, ADULT (CONTAINS: ADULT ELONGATED MASK, NEBULIZER BOTTLE 6ML, 7' O NEBULIZER SET, ADULT (CONTAINS: ADULT ELONGATED MASK, NEBULIZER BOTTLE 6ML, 7' OXYGEN TUBE W/ STANDARD-STANDARD CONNECTORS) GLOBAL HEALTHCARE GHC HEALTHCARE, INC.
7 00869112000175 0001 Hypersoniq PDA FLYp CONVEXITY SCIENTIFIC LLC
8 00869112000168 0002 Vibrating mesh nebulizer FLYp CONVEXITY SCIENTIFIC LLC
9 00869112000106 0001 Vibrating mesh nebulizer FLYp CONVEXITY SCIENTIFIC LLC
10 00865528000099 Sensor Model 2017-B Model 2017-B. The sensor is an accessory device intended for single-patient use Model 2017-B. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed DPI usage for Neohaler® devices.• The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the DPI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician, and healthcare providers. • The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their DPI and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians, and health care providers. • When used with a prescribed DPI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing DPI technique. • The Propeller System is intended to be used in populations from Child (>2 years) to Adult. • The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft. • The Propeller System may also be used in clinical trials where researchers need to know information about the use of DPI medication(s) by a participant. • The output of the Propeller System is not intended to diagnose or replace a diagnosis provided by a licensed physician. The Propeller System is not intended for use as an DPI dose counter, nor is it intended to indicate the quantity of medication remaining in an DPI. Propeller RECIPROCAL LABS CORPORATION
11 00865528000082 Sensor Model 2016-M-L The Propeller System includes the OTC Sensor Model 2016-M for MDI. The sensor is The Propeller System includes the OTC Sensor Model 2016-M for MDI. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed MDI usage.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the MDI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their respiratory medication(s) and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians and healthcare providers.When used with a prescribed MDI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing MDI technique.When used under the care of a physician with a prescribed MDI, or other inhaled medication, the system can be used to reduce the frequency of respiratory health symptoms and exacerbations by increasing adherence to MDI or other inhaled medications through the use of feedback such as reminders and notifications, and self-management education.The Propeller System is intended to be used in populations from Child (>2 years) to adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use of MDI or other inhaled medication(s) by a participant. Propeller RECIPROCAL LABS CORPORATION
12 00865528000075 Sensor Model 2016-M-S The Propeller System includes the OTC Sensor Model 2016-M for MDI. The sensor is The Propeller System includes the OTC Sensor Model 2016-M for MDI. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed MDI usage.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the MDI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their respiratory medication(s) and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians and healthcare providers.When used with a prescribed MDI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing MDI technique.When used under the care of a physician with a prescribed MDI, or other inhaled medication, the system can be used to reduce the frequency of respiratory health symptoms and exacerbations by increasing adherence to MDI or other inhaled medications through the use of feedback such as reminders and notifications, and self-management education.The Propeller System is intended to be used in populations from Child (>2 years) to adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use of MDI or other inhaled medication(s) by a participant. Propeller RECIPROCAL LABS CORPORATION
13 00865528000068 Sensor Model 2015-E The Propeller System includes the Propeller Sensor Model 2015-E. The sensor is a The Propeller System includes the Propeller Sensor Model 2015-E. The sensor is an accessory device intended for singlepatientuse to assist physicians and patients in recording and monitoring the actuations of prescribed DPI usage for theEllipta devices.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual userentry, to a remote storage system. With the Propeller Mobile Application the user can review information collected fromthe DPI sensor, and report and review symptoms and other information about their disease management and its impact.The user may also share their information with their caregivers, physician, and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users toreview the collected information and characteristics of their DPI and its use, to capture other patient-reported informationand outcomes, and to allow that information to be shared with their caregivers, physicians, and health care providers.When used with a prescribed DPI, the system can report on information captured during the normal course of use, such asthe time between actuations that can be helpful in assessing DPI technique.The Propeller System is intended to be used in populations from Child (>2 years) to Adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use of DPImedication(s) by a participant.The output of the Propeller System is not intended to diagnose or replace a diagnosis provided by a licensed physician.The Propeller System is not intended for use as an DPI dose counter, nor is it intended to indicate the quantity ofmedication remaining in an DPI. Propeller RECIPROCAL LABS CORPORATION
14 00865528000037 Sensor Model 2014-D The Propeller System includes the Propeller DPI Model 2014-D Sensor. The sensor The Propeller System includes the Propeller DPI Model 2014-D Sensor. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed DPI usage.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the DPI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their respiratory medication(s) and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians and healthcare providers.When used with a prescribed DPI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing DPI technique.When used under the care of a physician with a prescribed DPI, or other inhaled medication, the system can be used to reduce the frequency of respiratory health symptoms and exacerbations by increasing adherence to DPI or other inhaled medications through the use of feedback such as reminders and notifications, and self-management education.The Propeller System is intended to be used in populations from Child (>2 years) to adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use of MDI or other inhaled medication(s) by a participant. Propeller RECIPROCAL LABS CORPORATION
15 00865528000020 Sensor Model 2014-R The Propeller System includes the Propeller SMI Model 2014-R Sensor. The sensor The Propeller System includes the Propeller SMI Model 2014-R Sensor. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed SMI usage.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the SMI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their respiratory medication(s) and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians and healthcare providers.When used with a prescribed SMI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing SMI technique.When used under the care of a physician with a prescribed SMI, or other inhaled medication, the system can be used to reduce the frequency of respiratory health symptoms and exacerbations by increasing adherence to SMI or other inhaled medications through the use of feedback such as reminders and notifications, and self-management education.The Propeller System is intended to be used in populations from Child (>2 years) to adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use of MDI or other inhaled medication(s) by a participant. Propeller RECIPROCAL LABS CORPORATION
16 00865528000013 MDI 2 Sensor The Propeller System includes the Propeller MDI Model 2 OTC Sensor. The sensor i The Propeller System includes the Propeller MDI Model 2 OTC Sensor. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed MDI usage.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the MDI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their respiratory medication(s) and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians and healthcare providers.When used with a prescribed MDI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing MDI technique.When used under the care of a physician with a prescribed MDI, or other inhaled medication, the system can be used to reduce the frequency of respiratory health symptoms and exacerbations by increasing adherence to MDI or other inhaled medications through the use of feedback such as reminders and notifications, and self-management education.The Propeller System is intended to be used in populations from Child (>2 years) to adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use of MDI or other inhaled medication(s) by a participant. Propeller RECIPROCAL LABS CORPORATION
17 00863943000120 NB40 Aura Medical AURA MEDICAL
18 00860456000937 JLN-2300 AS Remedium International LLC REMEDIUM INTERNATIONAL LLC
19 00860456000920 JLN-2305 BS Remedium International LLC REMEDIUM INTERNATIONAL LLC
20 00860456000913 JLN-2320 AS Remedium International LLC REMEDIUM INTERNATIONAL LLC
21 00860004038115 white MCN-S600MD Compressor Nebulizer Machine WhiteFull UDI: (01)00860004038115(11)200701(10)120205006 Aerdilx PLATINUM EXPORTS PTY LTD
22 00860004038108 Blue MCN-S600MD Compressor Nebulizer Machine BlueFull UDI: (01)00860004038108(11)200701(10)120205006 Aerdilx PLATINUM EXPORTS PTY LTD
23 00860003079706 NEB002 Intelligent Mesh Nebulizer True Integral TRUE INTEGRAL INC
24 00860002180618 AH-04 AireHealth Nebulizer AIREHEALTH LLC
25 00860002180601 AH03 AireHealth Nebulizer AIREHEALTH LLC
26 00859105006345 Sensor Model 2018-S The Propeller System includes the Propeller Sensor Model 2018-S. The sensor is a The Propeller System includes the Propeller Sensor Model 2018-S. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed pMDI usage for theSymbicort device.The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual userentry, to a remote storage system. With the Propeller Mobile Application the user can review information collected fromthe pMDI sensor, and report and review symptoms and other information about their disease management and its impact.The user may also share their information with their caregivers, physician, and healthcare providers.The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users toreview the collected information and characteristics of their pMDI and its use, to capture other patient-reportedinformation and outcomes, and to allow that information to be shared with their caregivers, physicians, and health careproviders.When used with a prescribed pMDI, the system can report on information captured during the normal course of use, suchas the time between actuations that can be helpful in assessing pMDI technique.The Propeller System is intended to be used in populations from Child (>2 years) to Adult.The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.The Propeller System may also be used in clinical trials where researchers need to know information about the use ofpMDI medication(s) by a participant.The output of the Propeller System is not intended to diagnose or replace a diagnosis provided by a licensed physician.The Propeller System is not intended for use as an pMDI dose counter, nor is it intended to indicate the quantity ofmedication remaining in an pMDI. Propeller RECIPROCAL LABS CORPORATION
27 00857863007789 MCT-5H Methacholine Test Kit, HEPA Filter, 5 Test/CS Healthline, Medicator Maximizer, Methacholine MEDI/NUCLEAR CORPORATION, INC.
28 00857863007772 ARK-23 Asthma Rescue Kit, Adult Mask, HEPA Filter Healthline, ARK- Asthma Rescue Kit MEDI/NUCLEAR CORPORATION, INC.
29 00857863007765 ARK-27 Asthma Rescue Kit, Pediatric Mask, HEPA Filter Healthline, ARK - Asthma Rescue Kit MEDI/NUCLEAR CORPORATION, INC.
30 00857863007758 ARK-5 Asthma Rescue Kit, Pediatric, Bacteria Filter, w/ Mix & Mount Body Healthline, ARK - Asthma Rescue Kit, Mix & Mount MEDI/NUCLEAR CORPORATION, INC.
31 00857863007741 ARK-1 Asthma Rescue Kit, Adult, Bacteria Filter, w/ Mix & Mount Body Healthline, ARK - Asthma Rescue Kit, Mix & Mount MEDI/NUCLEAR CORPORATION, INC.
32 00857863007734 AM-603H Medicator Maximizer+Plus, No Neb, HEPA Filter Healthline, Medicator Maximizer MEDI/NUCLEAR CORPORATION, INC.
33 00857863007727 AM-602H Medicator Maximizer+Plus HEPA Healthline, Medicator Maximizer MEDI/NUCLEAR CORPORATION, INC.
34 00857863007710 AM-602 Medicator Maximizer+Plus Neb3A Healthline, Medicator Maximizer Plus MEDI/NUCLEAR CORPORATION, INC.
35 00856702006051 MVD-70-9 Replacement Pocket Neb Nebulizer Mouthpiece and Mask Adapter Pocket Neb MICROVAPOR DEVICES, LLC
36 00856702006037 MVD-70-8 Replacement Pocket Neb Nebulizer Medication Cups with Mouthpiece and Mask Adapter Pocket Neb MICROVAPOR DEVICES, LLC
37 00856702006020 MC-001 Medication chamber of the Nebulizer NA HEALTH & LIFE CO., LTD.
38 00856702006013 MVD-70 The MVD-70, Pocket Neb is an electronic vibrating mesh nebulizer designed to aer The MVD-70, Pocket Neb is an electronic vibrating mesh nebulizer designed to aerosolize liquid medications for inhalation by the patient. The device may be used with pediatric and adult patients in and out of the home environment. Pocket Neb MICROVAPOR DEVICES, LLC
39 00855944007611 ACDOA-1144 ACDOA-1144-100 Areta 14-Panel Drug Test Cup (100 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA Areta 14-Panel Drug Test Cup (100 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC Areta Multi-Drug Test Cup (100 tests kit) EASY HEALTHCARE CORPORATION
40 00855944007604 ACDOA-1144 ACDOA-1144-50 Areta 14-Panel Drug Test Cup (50 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA Areta 14-Panel Drug Test Cup (50 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC Areta Multi-Drug Test Cup (50 tests kit) EASY HEALTHCARE CORPORATION
41 00855944007598 ACDOA-1144 ACDOA-1144-10 Areta 14-Panel Drug Test Cup (10 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA, Areta 14-Panel Drug Test Cup (10 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC Areta Multi-Drug Test Cup (10 tests kit) EASY HEALTHCARE CORPORATION
42 00855944007581 ACDOA-6125B ACDOA-6125B-100 Areta 12 Panel Drug Test Cup (100 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZ Areta 12 Panel Drug Test Cup (100 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP Areta Multi-Drug Test Cup (100 tests kit) EASY HEALTHCARE CORPORATION
43 00855944007574 ACDOA-6125B ACDOA-6125B-50 Areta 12 Panel Drug Test Cup (50 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO Areta 12 Panel Drug Test Cup (50 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP Areta Multi-Drug Test Cup (50 tests kit) EASY HEALTHCARE CORPORATION
44 00855944007567 ACDOA-6125B ACDOA-6125B-10 Areta 12 Panel Drug Test Cup (10 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO Areta 12 Panel Drug Test Cup (10 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP Areta Multi-Drug Test Cup (10 tests kit) EASY HEALTHCARE CORPORATION
45 00855944007291 ACDOA-6125B ACDOA-6125B-25 Areta 12 Panel Drug Test Cup (25 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO Areta 12 Panel Drug Test Cup (25 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP Areta Multi-Drug Test Cup (25 tests kit) EASY HEALTHCARE CORPORATION
46 00855944007284 ACDOA-6125B ACDOA-6125B-5 Areta 12 Panel Drug Test Cup (5 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO, Areta 12 Panel Drug Test Cup (5 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP Areta Multi-Drug Test Cup (5 tests kit) EASY HEALTHCARE CORPORATION
47 00855944007215 ACDOA-1144 ACDOA-1144-25 Areta 14-Panel Drug Test Cup (25 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA Areta 14-Panel Drug Test Cup (25 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC Areta Multi-Drug Test Cup (25 tests kit) EASY HEALTHCARE CORPORATION
48 00855944007208 ACDOA-1144 ACDOA-1144-5 Areta 14-Panel Drug Test Cup (5 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,M Areta 14-Panel Drug Test Cup (5 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC Areta Multi-Drug Test Cup (5 tests kit) EASY HEALTHCARE CORPORATION
49 00853292007536 RTG-07106 RTG-07106 Nebu-Life Hand Held Nebulizer 6cc Cup, w/ Pediatric Aerosol Elongated Mask & 7 Nebu-Life Hand Held Nebulizer 6cc Cup, w/ Pediatric Aerosol Elongated Mask & 7' Tube (2.1m). Pediatric. The Jet Nebulizer Bottle Set is used to administer various aerosal treatments to adults and pediatric patients in both the homecare and hospital settings. Its use is indicated whenever a physician or healthcare professional administers or prescribes medical aerosol products to a patient using a Small Volume Nebulizer. Nebu-Life CUTTING EDGE HC BRANDS LLC
50 00853292007529 RTG-07105 RTG-07105 Nebu-Life Hand Held Nebulizer 6cc Cup, w/Adult Aerosol Elongated Mask & 7' Tube Nebu-Life Hand Held Nebulizer 6cc Cup, w/Adult Aerosol Elongated Mask & 7' Tube (2.1m). ADULT. The Jet Nebulizer Bottle Set is used to administer various aerosal treatments to adults and pediatric patients in both the homecare and hospital settings. Its use is indicated whenever a physician or healthcare professional administers or prescribes medical aerosol products to a patient using a Small Volume Nebulizer. Nebu-Life CUTTING EDGE HC BRANDS LLC