Other products from "SOUTHMEDIC INCORPORATED"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00620974002581 73-9015C 73-9015C Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
2 00620974001706 DWS12 DWS12 SutureSafe Set MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
3 10620974000638 OAT-4025-8 OAT-4025-8 OxyTrach Mask Adult O2 Aerosol with Nebulizer Kit CAF NEBULIZER (DIRECT PATIENT INTERFACE) NA
4 00620974002574 73-9022 73-9022 Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
5 00620974002567 73-9021 73-9021 Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
6 00620974002222 73-9020 73-9020 Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
7 00620974002208 73-9015 73-9015 Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
8 00620974002185 73-9011 73-9011 Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
9 00620974002161 73-9010 73-9010 Safety Scalpel with Southmedic Plus Surgical Blade GES BLADE, SCALPEL SPSS Disposable Scalpels
10 00620974001867 CZE07 CZE07 ABRA Silicone Cord Elastomer KGS RETENTION DEVICE, SUTURE Dynamic Tissue Systems™
11 00620974001799 DCNE-02 DCNE-02 DynaCleft Nasal Elevation System MZR TOPICAL APPROXIMATION SYSTEM Dynamic Tissue Systems™
12 00620974001782 DCNE-01 DCNE-01 DynaCleft Nasal Elevation System MZR TOPICAL APPROXIMATION SYSTEM Dynamic Tissue Systems™
13 00620974001775 DCX20 DCX20 DynaCleft Bilateral MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
14 00620974001768 DCX10 DCX10 DynaCleft Unilateral MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
15 00620974001751 DSX38 DSX38 DynaStretch Set MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
16 00620974001744 DSX24 DSX24 DynaStretch Set MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
17 00620974001737 DWC38 DWC38 DynaClose Set MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
18 00620974001720 DWC24 DWC24 DynaClose Set MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
19 00620974001713 DWS14 DWS14 SutureSafe Set MKY SYSTEM, SKIN CLOSURE Dynamic Tissue Systems™
20 10620974002342 SWC02 SWC02 ABRA Loop Cannulator MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE 1 Dynamic Tissue Systems™
21 10620974002335 SWC01 SWC01 Cannulator MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE 1 Dynamic Tissue Systems™
22 10620974002328 SWA07-20 SWA07-20 ABRA Button Tail KGS RETENTION DEVICE, SUTURE 1 Dynamic Tissue Systems™
23 10620974002311 AWC01/BOX AWC01/BOX Elastomer Retainer KGS RETENTION DEVICE, SUTURE 1 Dynamic Tissue Systems™
24 10620974002304 CWK-3 CWK-3 ABRA® Abdominal Wall Closure Set Extension KGS RETENTION DEVICE, SUTURE 1 Dynamic Tissue Systems™
25 10620974001932 CWKSR-S CWKSR-S Southmedic Surgical Retainer Small GZC Stimulator, neuromuscular, implanted 3 Dynamic Tissue Systems™
26 10620974001918 CWKSR-L CWKSR-L Southmedic Surgical Retainer Large GZC Stimulator, neuromuscular, implanted 3 Dynamic Tissue Systems™
27 10620974001857 CWK-H CWK-H ABRA® Abdominal Wall Closure Set H LRO General surgery tray 2 Dynamic Tissue Systems™
28 10620974001833 CWK-EX CWK-EX ABRA® Abdominal Wall Closure Set Extension LRO General surgery tray 2 Dynamic Tissue Systems™
29 10620974001826 CWK08 CWK08 ABRA® Abdominal Wall Closure Set LRO General surgery tray 2 Dynamic Tissue Systems™
30 10620974001819 CWK02A CWK02A ABRA® Surgical Skin Closure Set LRO General surgery tray 2 Dynamic Tissue Systems™
31 10620974001802 CWM02A CWM02A ABRA® Adhesive Skin Closure Set LRO General surgery tray 2 Dynamic Tissue Systems™
32 10620974001697 SMDIA-1100B SMDIA-1100B MDI Adaptor for use with or without dosage counters -22mm OD/15mm ID x 22mm ID ( MDI Adaptor for use with or without dosage counters -22mm OD/15mm ID x 22mm ID (Flow OD to ID) CAF NEBULIZER (DIRECT PATIENT INTERFACE) NA
33 10620974001673 SMDIA-1300 SMDIA-1300 MDI Adaptor for use with or without dosage counters - 15mm OD x 15mm ID (Flow OD to ID) CAF NEBULIZER (DIRECT PATIENT INTERFACE) NA
34 10620974001666 SMDIA-1200 SMDIA-1200 MDI Adaptor for use with or without dosage counters - 22 mm OD x 15 mm ID / 22 MDI Adaptor for use with or without dosage counters - 22 mm OD x 15 mm ID / 22 mm OD x 15 mm ID CAF NEBULIZER (DIRECT PATIENT INTERFACE) NA
35 10620974001642 NCD-2025-8 NCD-2025-8 Divided Nasal Cannula Adult with 7 ft O2 tube and 7 ft CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
36 10620974001635 SMDIA-1100 SMDIA-1100 MDI Adaptor for use with or without dosage counters -22 mm OD/ 11mm ID x 22mm ID MDI Adaptor for use with or without dosage counters -22 mm OD/ 11mm ID x 22mm ID (Flow OD to ID) CAF NEBULIZER (DIRECT PATIENT INTERFACE) NA
37 10620974001468 NCP-2025-8F NCP-2025-8F Pediatric CO2/O2 Nasal Cannula with 7ft O2 and CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
38 10620974001451 NCP-2025-14 NCP-2025-14 Pediatric CO2/O2 Nasal Cannula with 14ft O2 and 14ft CO2 Tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
39 10620974001444 NCP-2025-8 NCP-2025-8 Pediatric CO2/O2 Nasal Cannula with 7ft O2 and CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
40 10620974001437 NCP-2025-7 NCP-2025-7 Pediatric CO2/O2 Nasal Cannula with 7ft O2 and 3in CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
41 10620974001420 NCP-2025-6 NCP-2025-6 Pediatric CO2/O2 Nasal Cannula with 4in O2 and 3in CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
42 10620974001376 NC-2025-8F NC-2025-8F CO2/O2 Nasal Cannula with 7ft O2 and CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
43 10620974001314 CO2SL055-8MM CO2SL055-8MM 10 ft Sampling Line with Male Connectors CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
44 10620974001307 CO2SL055-8MF CO2SL055-8MF 10 ft Sampling Line with Male and Female Connectors CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
45 10620974001277 NC-2025-7 NC-2025-7 CO2/O2 Nasal Cannula with 7ft O2 and 3in CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
46 10620974001260 NC-2025-6 NC-2025-6 CO2/O2 Nasal Cannula with 4in O2 and 3in CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
47 10620974001192 OK-2125-8SLM OK-2125-8SLM OxyKid Pediatric Mask ETCO2, 7ft oxygen tubing, 8ft sampling line with male connector CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE OxyKid™
48 10620974001147 NC-2025-8 NC-2025-8 CO2/O2 Nasal Cannula with 7ft O2 and CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
49 10620974001130 NC-2025-14 NC-2025-14 CO2/O2 Nasal Cannula with 14ft O2 and CO2 tube CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE NA
50 10620974001109 SMDIA-1000 SMDIA-1000 MDI Adaptor for use with or without dosage counters -22 mm ID x 22mm OD/15mm ID MDI Adaptor for use with or without dosage counters -22 mm ID x 22mm OD/15mm ID (Flow ID to OD) CAF NEBULIZER (DIRECT PATIENT INTERFACE) NA
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