Other products from "COMPASS HEALTH BRANDS CORP."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00854875008049 70256FSA Large Face LCD Fast Read Digital Thermometer FLL Thermometer, Electronic, Clinical 2 Apex
2 00815067043880 GEL-182 IMP Cushion, Wheelchair 1 Meridian Medical Gel Wheelchair Cushion - 18 x 16 x 2
3 00815067043798 X1SAPM5306 MER-SAPM PUMP - 8 LPM/350 LB CAP FNM Mattress, Air Flotation, Alternating Pressure 2 MERIDIAN
4 00815067043743 X1SAPM5301 MER-SAPM53 MATTRESS ONLY FNM Mattress, Air Flotation, Alternating Pressure 2 MERIDIAN
5 00815067043682 X1SAPM201 MER-SAPM2 MATTRESS ONLY FNM Mattress, Air Flotation, Alternating Pressure 2 MERIDIAN
6 00815067043378 4840-54 54'' APM BARIATRIC SYSTEM FNM Mattress, Air Flotation, Alternating Pressure MERIDIAN
7 00815067043309 HDC-WC1816 IMP Cushion, Wheelchair 1 Wedge Cushion - 18 x 16
8 00815067013135 E100-6R Viverity Pain Relief Pad, NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter N/A
9 00813520013029 WS3147 Snaps-Black with Pigtail IKD Cable, Electrode 2 N/A
10 00813520012800 EP2020RW2 Electrode - Relief Wrap - 2x2 GXY Electrode, Cutaneous N/A
11 00813520011919 EP15140WF2 Electrode - Poly - 1.5x14 - GXY Electrode, Cutaneous N/A
12 00813520011896 EF2040WF2 Electrode - Foil - 2x4 - White GXY Electrode, Cutaneous N/A
13 00813520011889 EF2040TC2 Electrode - Foil - 2x4 - Tan GXY Electrode, Cutaneous N/A
14 00813520011568 DA1812 TENS AA - Digital TENS Unit GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief 2 N/A
15 00813520011339 EP2035BC2 Electrode - Poly - 2x3.5 - GXY Electrode, Cutaneous N/A
16 00813520011315 E1P2020BC2 Self-Adhering Electrodes, 2 GXY Electrode, Cutaneous N/A
17 00813520010493 EF2035WC2 Electrode - Foil - 2x3.5 - GXY Electrode, Cutaneous N/A
18 00813520010363 E1P3000WC2 Electrode - Poly - 3 - White GXY Electrode, Cutaneous N/A
19 00813520010356 E1P2035WC2 Electrode - Poly - 2x3.5 - GXY Electrode, Cutaneous N/A
20 00813520010349 E1P2020WC2 Electrode, Poly Bag 2 x 2 white cloth GXY Electrode, Cutaneous N/A
21 00813520010332 E1P1515WC2 Electrode - Poly - 1.5x1.5 - GXY Electrode, Cutaneous N/A
22 00813520010240 WW3005 Lead Wire - Standard 45 IKD Cable, Electrode N/A
23 00813520010141 EF2035WF2 Electrodes, Foil Bag, 2.0 x GXY Electrode, Cutaneous N/A
24 00813520010134 EF2035TC2 Electrode - Foil - 2x3.5 - Tan GXY Electrode, Cutaneous N/A
25 00813520010110 EPBUTTWF2 Electrode, 4 x 6 Butterfly GXY Electrode, Cutaneous N/A
26 00813520010059 EF2000WF2 Electrode - Foil - 2 - White GXY Electrode, Cutaneous N/A
27 00813520010035 EF2020WF2 Electrode - Foil - 2x2 - White GXY Electrode, Cutaneous N/A
28 00092237902554 410-012-HMR CM4 Winner Evo Device WITH HAMMER, electrodes, gel and lead wires IMI,GZJ,IPF,LIH Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat,Stimulator, Nerve Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat,Stimulator, Nerve, Transcutaneous, For Pain Relief,Stimulator, Muscle, Powered,Interferential Current Therapy 2 CM4 Winner Evo Device WITH HAMMER
29 00092237623473 DO1009 Hivadot with accessories, deep oscillation device ISA Massager, Therapeutic, Electric 1 HIVADOT
30 00092237622292 400-8722 MultiStim (TR) 2", Round Cloth, 4/pk GXY Electrode, Cutaneous MultStim 2" Round, Cloth
31 00092237622100 DT7202-GLOVE Tens 7000 Conductive Glove includes (1) pair of gloves, snap lead wires, insert Tens 7000 Conductive Glove includes (1) pair of gloves, snap lead wires, insert and pack of 3" round electrodes GXY Electrode, Cutaneous Tens 7000 Conductive Glove
32 00092237622094 DQ8222 Richmar TheraTouch CX2 GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief 2 TheraTouch
33 00092237622049 DT7202-SLEEVE Tens 7000 Conductive Sleeves includes (1) pair of sleeves, snap lead wires, inse Tens 7000 Conductive Sleeves includes (1) pair of sleeves, snap lead wires, insert and pack of 3" round electrodes GXY Electrode, Cutaneous Tens 7000 Conductive Sleeves
34 00092237621028 EF1200TC2 1.25" round tan cloth elecs GXY Electrode, Cutaneous Roscoe elecs
35 00092237619452 ESW-9050 eswallow GXY Electrode, Cutaneous 2 Eswallow
36 00092237619445 ESW-9100 eSwallow GXY Electrode, Cutaneous Eswallow
37 00092237619438 ESW-9030 eSwallow GXY Electrode, Cutaneous Eswallow
38 00092237619421 ESW-9010 eSwallow GXY Electrode, Cutaneous Eswallow
39 00092237619131 EP2020TC2A Electrode - 2x2 - Tan Cloth GXY Electrode, Cutaneous N/A
40 00092237618332 EP3000RR7 3 Round - Red Rubber GXY Electrode, Cutaneous N/A
41 00092237618325 EP2000RR7 2 " round red rubber electrodes GXY Electrode, Cutaneous N/A
42 00092237618318 EP2000BR7 2 " round black rubber electrodes GXY Electrode, Cutaneous N/A
43 00092237618288 ESW-9960 eSwallow Youth NMES Unit IPF Stimulator, Muscle, Powered 2 Eswallow
44 00092237618271 ESW-9050 eSwallow GXY Electrode, Cutaneous Eswallow
45 00092237618264 ESW-9100 eSwallow GXY Electrode, Cutaneous Eswallow
46 00092237618257 ESW-9030 eSwallow GXY Electrode, Cutaneous Eswallow
47 00092237618240 ESW-9010 eSwallow GXY Electrode, Cutaneous Eswallow
48 00092237617496 WW7360 Church Key Lead Wire style IKD Cable, Electrode N/A
49 00092237617472 WW6012 UltraTENS II Leadwire - Single IKD Cable, Electrode 2 N/A
50 00092237617465 WW6000 TOP TENS White Lead Wires IKD Cable, Electrode N/A
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