No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00085412004839 | 2N3349 | 2N3349 | Non-DEHP High Flow Rate Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
2 | 00085412007670 | 5C4462 | 5C4462 | This set is intended for use with a Baxter transfer set for peritoneal dialysis This set is intended for use with a Baxter transfer set for peritoneal dialysis patients requiring a sterile container for drainage. (i.e. CCPD patients doing a daytime exchange or CAPD patients who have disconnected between exchanges). | FKX | SYSTEM, PERITONEAL, AUTOMATIC DELIVERY | 2 | Empty Sterile Container |
3 | 00085412004808 | 2N3346 | 2N3346 | Non-DEHP High Flow Rate Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
4 | 00085412004983 | 2N3399 | 2N3399 | Injection Site | FPA | Set, administration, intravascular | 2 | INTERLINK |
5 | 00085412004976 | 2N3395 | 2N3395 | Universal Vial Adapter | LHI | Set, i.V. Fluid transfer | 2 | INTERLINK |
6 | 00085412004945 | 2N3379 | 2N3379 | Injection Site | FPA | Set, administration, intravascular | 2 | INTERLINK |
7 | 00085412004921 | 2N3376 | 2N3376 | Non-DEHP Y-Type Catheter Extension Set, 2 Injection Sites, Male Luer Lock Adapter | FPA | Set, administration, intravascular | INTERLINK | |
8 | 00085412004914 | 2N3375 | 2N3375 | Non-DEHP Catheter Extension Set, Injection Site, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | INTERLINK |
9 | 00085412004907 | 2N3374 | 2N3374 | Non-DEHP Catheter Extension Set, Injection Site, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | INTERLINK |
10 | 00085412004891 | 2N3373 | 2N3373 | Non-DEHP I.V. Connector Loop, Injection Site, Male Luer Lock with Rotating Collar | FPA | Set, administration, intravascular | 2 | INTERLINK |
11 | 00085412004877 | 2N3371 | 2N3371 | Non-DEHP Y-Type Catheter Extension Set, 2 Injection Sites, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | INTERLINK |
12 | 00085412004846 | 2N3350 | 2N3350 | Non-DEHP MICRO-VOLUME Extension Set, 0.2 Micron Downstream Filter, Male Luer Lock Adapter | FPB | Filter, infusion line | 2 | NA |
13 | 00085412004815 | 2N3347 | 2N3347 | Non-DEHP MICRO-VOLUME Extension Set, 0.2 Micron Downstream Filter, Male Luer Lock Adapter | FPB | Filter, infusion line | 2 | NA |
14 | 00085412004785 | 2N3343 | 2N3343 | Non-DEHP T-Connector Extension Set, T Housing, Retractable T-Connector, Injection Site | FPA | Set, administration, intravascular | 2 | INTERLINK |
15 | 00085412004778 | 2N3342 | 2N3342 | Non-DEHP Three Lead Catheter Extension Set, 0.2 Micron Filter, Male Luer Lock Adapter | FPB | Filter, infusion line | 2 | NA |
16 | 00085412004761 | 2N3341 | 2N3341 | Non-DEHP Three Lead Extension Set, Injection Site, Male Luer Lock Adapter | FPA | Set, administration, intravascular | INTERLINK | |
17 | 00085412004754 | 2N3340 | 2N3340 | Non-DEHP T-Connector Extension Set, T housing, Retractable T-Connector | FPA | Set, administration, intravascular | 2 | INTERLINK |
18 | 00085412004747 | 2N3339 | 2N3339 | Non-DEHP T-Connector Extension Set, T Housing, Retractable T-Connector | FPA | Set, administration, intravascular | 2 | INTERLINK |
19 | 00085412004716 | 2N3333 | 2N3333 | Non-DEHP T-Connector Catheter Extension Set, T-Housing, 0.2 Micron Filter, Rotat Non-DEHP T-Connector Catheter Extension Set, T-Housing, 0.2 Micron Filter, Rotating T-Connector | FPB | Filter, infusion line | 2 | INTERLINK |
20 | 00085412004662 | 2N3328 | 2N3328 | Non-DEHP T-Connector Extension Set, T Housing, Rotating T-Connector | FPA | Set, administration, intravascular | 2 | INTERLINK |
21 | 00085412004655 | 2N3327 | 2N3327 | Non-DEHP T-Connector Extension Set, T Housing, Rotating T-Connector | FPA | Set, administration, intravascular | 2 | INTERLINK |
22 | 00085412004648 | 2N3326 | 2N3326 | Non-DEHP T-Connector Extension Set, T Housing, Male Luer Slip T-Connector | FPA | Set, administration, intravascular | 2 | INTERLINK |
23 | 00085412004617 | 2N1206 | 2N1206 | Non-DEHP Catheter Extension Set, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | NA |
24 | 00085412004532 | 2N1191 | 2N1191 | Non-DEHP Y-Type Catheter Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
25 | 00085412004358 | 2C9292 | 2C9292 | Lever Lock Cannula with Check Valve | FPA | Set, administration, intravascular | 2 | INTERLINK |
26 | 00085412004259 | 2C9218 | 2C9218 | Universal Anesthesia Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
27 | 00085412004235 | 2C9216 | 2C9216 | Anesthesia Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
28 | 00085412004198 | 2C9203 | 2C9203 | Microbore Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
29 | 00085412004174 | 2C9201 | 2C9201 | Microbore Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
30 | 00085412004136 | 2C7627 | 2C7627 | Y-Type Blood/Solution Set with Standard Blood Filter, 170 to 260 Micron Filter, Y-Type Blood/Solution Set with Standard Blood Filter, 170 to 260 Micron Filter, Male Luer Lock Adapter with Retractable Collar | BRZ | Set, blood transfusion | 2 | NA |
31 | 00085412004112 | 2C7554 | 2C7554 | Solution Set, Male Luer Lock Adapter with Retractable Collar For Epidural Use | FPA | Set, administration, intravascular | 2 | NA |
32 | 00085412004006 | 2C6720 | 2C6720 | Y-Type Blood/Solution Set with Standard Blood Filter, 170 to 260 Micron Filter, Y-Type Blood/Solution Set with Standard Blood Filter, 170 to 260 Micron Filter, Injection Site, Male Luer Lock Adapter | BRZ | Set, blood transfusion | 2 | INTERLINK |
33 | 00085412003993 | 2C6671 | 2C6671 | Extension Set, 0.2 Micron Filter Injection Site, Male Luer Lock Adapter with Ret Extension Set, 0.2 Micron Filter Injection Site, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | INTERLINK |
34 | 00085412003962 | 2C6612 | 2C6612 | Extension Set, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | INTERLINK |
35 | 00085412003955 | 2C6606 | 2C6606 | Extension Set, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | INTERLINK |
36 | 00085412003917 | 2C6227 | 2C6227 | Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
37 | 00085412003900 | 2C6226 | 2C6226 | Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
38 | 00085412003863 | 2C6218 | 2C6218 | Three Gang Large Bore Stopcock Manifold with Rotating Male Luer Lock | FPA,FMG | Set, administration, intravascular,Stopcock, i.V. Set | 2 | NA |
39 | 00085412003856 | 2C6217 | 2C6217 | Two Gang Large Bore Stopcock Manifold with Rotating Male Luer Lock | FMG,FPA | Stopcock, i.V. Set,Set, administration, intravascular | 2 | NA |
40 | 00085412003849 | 2C5687 | 2C5687 | Minivolume Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
41 | 00085412003832 | 2C5685 | 2C5685 | Minivolume Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
42 | 00085412003818 | 2C5641 | 2C5641 | Extension Set, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | NA |
43 | 00085412003252 | 2B8066 | 2B8066 | Additive Cap | KPE | CONTAINER, I.V. | N/A | |
44 | 00085412002996 | 2C9221 | 2C9221 | High Flow Rate Extension Set, Luer Lock Adapters | FPA | Set, administration, intravascular | 2 | NA |
45 | 00085412002972 | 2C9219 | 2C9219 | Minivolume Extension Set, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | NA |
46 | 00085412002576 | 2C7451 | 2C7451 | Secondary Medication Set, Hanger, Lever Lock cannula, Male Luer Lock Adapter | FPA | Set, administration, intravascular | 2 | INTERLINK |
47 | 00085412002422 | 2C6891 | 2C6891 | Extension Set with CONTROL-A-FLO Regulator, Injection Site, Male Luer Lock Adapt Extension Set with CONTROL-A-FLO Regulator, Injection Site, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | INTERLINK/CONTROL-A-FLO |
48 | 00085412002408 | 2C6714 | 2C6714 | Y-Type Blood/Solution Set with Large Standard Blood Filter, 170 to 260 Micron Fi Y-Type Blood/Solution Set with Large Standard Blood Filter, 170 to 260 Micron Filter, 2 Injection Sites, Male Luer Lock Adapter | BRZ | Set, blood transfusion | 2 | INTERLINK |
49 | 00085412002361 | 2C6631 | 2C6631 | Extension Set, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar | FPA | Set, administration, intravascular | 2 | INTERLINK |
50 | 00085412002347 | 2C6607 | 2C6607 | Extension Set, Large Bore Stopcock with Rotating Male Luer Lock, 2 Injection Sit Extension Set, Large Bore Stopcock with Rotating Male Luer Lock, 2 Injection Sites, Luer Lock Adapter with Retractable Collar | FMG,FPA | Stopcock, i.V. Set,Set, administration, intravascular | 2 | INTERLINK |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00085412639505 | 955630 | 955630 | The TherMax blood warmer is an accessory device intended for use with the PrisMa The TherMax blood warmer is an accessory device intended for use with the PrisMax system and appropriate blood warmer compatible Prismaflex sets for the therapy in use. The blood warmer heats the return blood flow during a PrisMax system treatment in order to replace heat lost to the atmosphere and replacement fluids. | therMaxTherMax Blood Warmer | BAXTER HEALTHCARE CORPORATION |
2 | 00085412639499 | 955626 | 955626 | The PrisMax control unit is a software controlled single patient device that per The PrisMax control unit is a software controlled single patient device that performs Continuous Renal Replacement Therapy and Therapeutic Plasma Exchange Therapy | prisMaxPrisMax System | BAXTER HEALTHCARE CORPORATION |
3 | 00085412090429 | XPH210 | H25606A | Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or ch Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Xenium XPH Dialyzer | BAXTER INTERNATIONAL INC. |
4 | 00085412090412 | XPH190 | H25605A | Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or ch Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Xenium XPH Dialyzer | BAXTER INTERNATIONAL INC. |
5 | 00085412090405 | XPH170 | H25604A | Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or ch Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Xenium XPH Dialyzer | BAXTER INTERNATIONAL INC. |
6 | 00085412090399 | XPH150 | H25603A | Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or ch Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Xenium XPH Dialyzer | BAXTER INTERNATIONAL INC. |
7 | 00085412090382 | XPH130 | H25602A | Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or ch Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Xenium XPH Dialyzer | BAXTER INTERNATIONAL INC. |
8 | 00085412090375 | XPH110 | H25601A | Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or ch Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Xenium XPH Dialyzer | BAXTER INTERNATIONAL INC. |
9 | 00085412071275 | 150 | 5M2119 | Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients w Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Exeltra Dialyzer | BAXTER INTERNATIONAL INC. |
10 | 00085412071244 | 210 | 5M2132 | Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients w Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Exeltra Dialyzer | BAXTER INTERNATIONAL INC. |
11 | 00085412071220 | 190 | 5M2121 | Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients w Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Exeltra Dialyzer | BAXTER INTERNATIONAL INC. |
12 | 00085412071213 | 170 | 5M2120 | Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients w Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. | Exeltra Dialyzer | BAXTER INTERNATIONAL INC. |
13 | B815SM2000030 | SM-200-003 | SM-200-003 | The SAMI Hemofiltration Cassette is provided sterile, single use only, and has a The SAMI Hemofiltration Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. | SAMI Hemofiltration Cassette | DIALCO MEDICAL INC |
14 | B815SM1000030 | SM-100-003 | SM-100-003 | The SAMI RRT Unit is a software controlled device that performs the following fu The SAMI RRT Unit is a software controlled device that performs the following functions: - Primes the disposable cassette automatically,- Pumps blood through the blood flow path of the disposable cassette,- Delivers anticoagulant into the blood flow path,- Pumps sterile infusion solutions into the blood flow path of the disposable according to therapy in use,- Pumps sterile dialysate into the fluid compartment of the filter in RRT therapies,- Controls the patient fluid removal or plasma loss according to the therapy in use,- Monitors the system and alerts the operator of abnormal situations through alarms.The SAMI RRT Unit has a touchscreen interface that provides operating instructions to the user. The system is used in conjunction with the cassette tubing set. | SAMI RRT System | DIALCO MEDICAL INC |
15 | B815SA400000 | SA-400-00 | SA-400-00 | The SAMI RRT Cassette is provided sterile, single use only, and has a non-toxic, The SAMI RRT Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. | SAMI RRT Cassette | DIALCO MEDICAL INC |
16 | B815SA300000 | SA-300-00 | SA-300-00 | The SAMI Hemofiltration Cassette is provided sterile, single use only, and has a The SAMI Hemofiltration Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. | SAMI Hemofiltration Cassette | DIALCO MEDICAL INC |
17 | B815SA100010 | SA-100-01 | SA-100-01 | The SAMI RRT Unit is a software controlled device that performs the following fu The SAMI RRT Unit is a software controlled device that performs the following functions: - Primes the disposable cassette automatically,- Pumps blood through the blood flow path of the disposable cassette,- Delivers anticoagulant into the blood flow path,- Pumps sterile infusion solutions into the blood flow path of the disposable according to therapy in use,- Pumps sterile dialysate into the fluid compartment of the filter in RRT therapies,- Controls the patient fluid removal or plasma loss according to the therapy in use,- Monitors the system and alerts the operator of abnormal situations through alarms.The SAMI RRT Unit has a touchscreen interface that provides operating instructions to the user. The system is used in conjunction with the cassette tubing set. | SAMI RRT | DIALCO MEDICAL INC |
18 | B815DM850000 | DM-850-00 | DM-850-00 | The DIMI RRT System is a software controlled device that performs the following The DIMI RRT System is a software controlled device that performs the following functions: - Primes the disposable cassette automatically,- Pumps blood through the blood flow path of the disposable cassette,- Delivers anticoagulant into the blood flow path,- Pumps sterile infusion solutions into the blood flow path of the disposable according to therapy in use,- Pumps sterile dialysate into the fluid compartment of the filter in RRT therapies,- Controls the patient fluid removal or plasma loss according to the therapy in use,- Monitors the system and alerts the operator of abnormal situations through alarms.The DIMI RRT System has a touchscreen interface that provides operating instructions to the user. The system is used in conjunction with the cassette tubing set. | DIMI RRT System | DIALCO MEDICAL INC |
19 | B815DI400000 | DI-400-00 | DI-400-00 | The DIMI RRT Cassette is provided sterile, single use only, and has a non-toxic, The DIMI RRT Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. | DIMI RRT Cassette | DIALCO MEDICAL INC |
20 | B173SM2000030 | SM-200-003 | SM-200-003 | The SAMI Hemofiltration Cassette is provided sterile, single use only, and has a The SAMI Hemofiltration Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. | SAMI Hemofiltration Cassette | SPECTRAL MEDICAL INC |
21 | B173SM1000030 | SM-100-003 | SM-100-003 | The SAMI RRT Unit is a software controlled device that performs the following fu The SAMI RRT Unit is a software controlled device that performs the following functions:- Primes the disposable cassette automatically.- Pumps blood through the blood flow path of the disposable cassette.- Delivers anticoagulant into the blood flow path.- Pumps sterile infusion solutions into the blood flow path of the disposable according to therapyin use.- Pumps sterile dialysate into the fluid compartment of the filter in RRT therapies.- Controls the patient fluid removal or plasma loss according to the therapy in use.- Monitors the system and alerts the operator to abnormal situations through alarms.The SAMI RRT Unit has a touchscreen interface that provides operating instructions to the user. The system is used in conjunction with the Cassette tubing set. | SAMI RRT | SPECTRAL MEDICAL INC |
22 | B173SA400000 | SA-400-00 | SA-400-00 | The SAMI RRT Cassette is provided sterile, single use only, and has a non-toxic, The SAMI RRT Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure.The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. | SAMI RRT Cassette | SPECTRAL MEDICAL INC |
23 | 37332414107728 | 800541 | 800541 | The MARS Treatment Kit Type 1116/1 X-MARS is a set of disposable items to be use The MARS Treatment Kit Type 1116/1 X-MARS is a set of disposable items to be used with the MARS Monitor 1TC in combination with the Prismaflex device (produced by Gambro Lundia AB) for MARS therapy. | MARS TREATMENT KIT TYPE 1116/1 - X-MARS US | GAMBRO AB |
24 | 37332414106936 | 800437 | 800437 | The MARS Monitor is a mechanical detoxification device used in conjunction with The MARS Monitor is a mechanical detoxification device used in conjunction with a renal replacement therapy system (companion device) for the removal of dialyzable (unbound) toxins, which are either water-soluble or, in the bound form, associated with serum albumin. | MARS Monitor | GAMBRO AB |
25 | 20860113000656 | 2.0 | CLR 2.0 | The SeaStar CLR 2.0 hemofilter is indicated for use in patients with fluid overl The SeaStar CLR 2.0 hemofilter is indicated for use in patients with fluid overload, uremia and/or electrolyte disturbances associated with oligoanuria acute renal failure. It may also be used when removal of excess fluid is indicated, such as patients in pulmonary edema or congestive heart failure refractory to diuretic therapy. | CLR | SEASTAR MEDICAL, INC. |
26 | 20850001011024 | PN-0000503 | ST-100 | Tablo Straws | OUTSET MEDICAL, INC. | |
27 | 10853072007289 | 210104 | 210104 | For use with the Aquadex System. The Aquadex System is indicated for: Continuous For use with the Aquadex System. The Aquadex System is indicated for: Continuous ultrafiltration therapy for temporary (up to 8 hours) or extended (longer than 8 hours in patients who require hospitalization) use in adult and pediatric patients weighing 20 kilograms or more whose fluid overload is unresponsive to medical management, including diuretics. All treatments must be administered within an outpatient or inpatient clinical setting by a healthcare provider, under physician prescription, both of whom having received training in extracorporeal therapies. | AquaFlexFlow UF 500 Plus - 24 Hr | NUWELLIS INC. |
28 | 10853072007128 | 114157 | 114157 | For use with the Aquadex System. The Aquadex System is indicated for: Continuous For use with the Aquadex System. The Aquadex System is indicated for: Continuous ultrafiltration therapy for temporary (up to 8 hours) or extended (longer than 8 hours in patients who require hospitalization) use in adult and pediatric patients weighing 20 kilograms or more whose fluid overload is unresponsive to medical management, including diuretics. All treatments must be administered within an outpatient or inpatient clinical setting by a healthcare provider, under physician prescription, both of whom having received training in extracorporeal therapies. | AquaFlexFlow UF 500 | NUWELLIS INC. |
29 | 10853072007111 | 114156 | 114156 | For use with the Aquadex System. The Aquadex System is indicated for: Continuous For use with the Aquadex System. The Aquadex System is indicated for: Continuous ultrafiltration therapy for temporary (up to 8 hours) or extended (longer than 8 hours in patients who require hospitalization) use in adult and pediatric patients weighing 20 kilograms or more whose fluid overload is unresponsive to medical management, including diuretics. All treatments must be administered within an outpatient or inpatient clinical setting by a healthcare provider, under physician prescription, both of whom having received training in extracorporeal therapies. | AquaFlexFlow UF 500 Plus | NUWELLIS INC. |
30 | 10853072007104 | 120100 | 120100 | The Aquadex SmartFlow System is indicated for: Continuous ultrafiltration therap The Aquadex SmartFlow System is indicated for: Continuous ultrafiltration therapy for temporary (up to 8 hours) or extended (longer than 8 hours in patients who require hospitalization) use in adult and pediatric patients weighing 20 kilograms or more whose fluid overload is unresponsive to medical management, including diuretics. All treatments must be administered within an outpatient or inpatient clinical setting by a healthcare provider, under physician prescription, both of whom having received training in extracorporeal therapies. | Aquadex SmartFlow Console | NUWELLIS INC. |
31 | 10853072007074 | 114158 | 114158 | The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration tr The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy, and extended (longer than 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy and require hospitalization. | Aquadex FlexFlow | NUWELLIS INC. |
32 | 10853072007029 | UF 500-HCT | 114156 | The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration tr The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy, and extended (longer than 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy and require hospitalization. | Blood Circuit Set | NUWELLIS INC. |
33 | 10853072007005 | UF 500 | 114157 | The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration tr The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy, and extended (longer than 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy and require hospitalization. | Blood Circuit Set | NUWELLIS INC. |
34 | M535SSK5350 | SSK-535 | NXSTAGE SPEEDSWAP EXPRESS KIT | NXSTAGE MEDICAL, INC. | ||
35 | M535SLE3011M30980 | SLE-3011M3098 | Streamline Express Dialyzer with Preattached Tubing Set For B.Braun Dialog Serie | MEDISYSTEMS CORPORATION | ||
36 | M535SLE3010M30960 | SLE-3010M3096 | Streamline Express Dialyzer with Preattached Tubing Set For B.Braun Dialog Serie | MEDISYSTEMS CORPORATION | ||
37 | M535SLE3000M30950 | SLE-3000M3095 | Streamline Express Dialyzer with Pre-attached Tubing Set For Fresenius 2008 Seri | MEDISYSTEMS CORPORATION | ||
38 | M535NX3302A0 | NX3302-A | NX3302-A | NXView Touch Monitor | NXSTAGE MEDICAL, INC. | |
39 | M535NX1274A0 | NX1274-A | NXVIEW TOUCH SCREEN | NXSTAGE MEDICAL, INC. | ||
40 | M535NX12740 | NX1274 | NXVIEW TOUCH SCREEN | NXSTAGE MEDICAL, INC. | ||
41 | M535NX10005A0 | NX1000-5-A | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
42 | M535NX100050 | NX1000-5 | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
43 | M535NX100040 | NX1000-4 | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
44 | M535NX10003CAN0 | NX1000-3-CAN | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
45 | M535NX10003A0 | NX1000-3-A | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
46 | M535NX100030 | NX1000-3 | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
47 | M535NX100020 | NX1000-2 | NXSTAGE SYSTEM ONE | NXSTAGE MEDICAL, INC. | ||
48 | M535NX100016A0 | NX1000-16-A | VersiHD | NXSTAGE MEDICAL, INC. | ||
49 | M535NX1000160 | NX1000-16 | VersiHD | NXSTAGE MEDICAL, INC. | ||
50 | M535NX100010B0 | NX1000-10-B | VersiHD | NXSTAGE MEDICAL, INC. |