No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00841911102472 | 4010-05-08-T4 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | Mammotome HydroMARK | |
2 | 00841911102465 | 4010-05-08-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | Mammotome HydroMARK | |
3 | 00841911102441 | 4010-05-10-T4 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | Mammotome HydroMARK | |
4 | 00841911102434 | 4010-05-10-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | Mammotome HydroMARK | |
5 | 00841911102427 | 4010-05-10-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | Mammotome HydroMARK | |
6 | 00841911102397 | 4010-05-08-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | Mammotome HydroMARK | |
7 | 00841911101703 | MEH1 | "Holster(tetherless vacuum-assisted biopsy system)" | KNW | Instrument, Biopsy | 2 | Mammotome elite | |
8 | 00841911101666 | MAM3014 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome CORMARK | |
9 | 00841911101635 | MMK1001 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome revolve mammomark | |
10 | 00841911101260 | ADT08S | Universal Targeting Set - Short | KNW | Instrument, Biopsy | 2 | Mammotome MI | |
11 | 00841911101253 | ADP08S | Bladeless Probe with Tube Set - Short | KNW | Instrument, Biopsy | 2 | Mammotome MI | |
12 | 00841911100898 | MEP13 | Probe | KNW | Instrument, Biopsy | 2 | Mammotome elite | |
13 | 00841911100881 | MEP10 | Probe | KNW | Instrument, Biopsy | 2 | Mammotome elite | |
14 | 00841911100874 | MEI13 | Introducer Stylet | KNW | Instrument, Biopsy | 2 | Mammotome elite | |
15 | 00841911100867 | MEI10 | Introducer Stylet | KNW | Instrument, Biopsy | 2 | Mammotome elite | |
16 | 00841911100850 | MEH1 | Holster (tetherless vacuum-assisted biopsy system) | KNW | Instrument, Biopsy | 2 | Mammotome elite | |
17 | 00841911100515 | MMK1002 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome revolve mammomark | |
18 | 00841911100485 | MMK0802 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome revolve mammomark | |
19 | 00841911100461 | MAM3015 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome CORMARK | |
20 | 00841911100454 | MAM3014 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome CORMARK | |
21 | 00841911101079 | MRT11X | MR Targeting Set - Long | KNW | Instrument, Biopsy | Mammotome MR | ||
22 | 00841911101697 | 4010-02-15-S1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
23 | 00841911101680 | MRM4008 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome MAMMOMARK | |
24 | 00841911101673 | MRM4002 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome MAMMOMARK | |
25 | 00841911101598 | MAM3001 | Biopsy Site Identifier | NEU,FZP | Marker, Radiographic, Implantable,Clip, Implantable | 2 | Mammotome MAMMOMARK | |
26 | 00841911101574 | 4010-04-09-T4 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
27 | 00841911101567 | 4010-04-09-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
28 | 00841911101550 | 4010-04-09-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
29 | 00841911101543 | 4010-04-09-S3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
30 | 00841911101536 | 4010-03-15-T3-SHORT | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
31 | 00841911101529 | 4010-03-15-T1-SHORT | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
32 | 00841911101512 | 4010-03-09-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
33 | 00841911101505 | 4010-03-09-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
34 | 00841911101499 | 4010-02-18-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
35 | 00841911101482 | 4010-02-15-T4 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
36 | 00841911101475 | 4010-02-15-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
37 | 00841911101468 | 4010-02-15-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
38 | 00841911101451 | 4010-02-15-S3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
39 | 00841911101444 | 4010-01-11-T4 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
40 | 00841911101437 | 4010-01-11-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
41 | 00841911101420 | 4010-01-11-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
42 | 00841911101413 | 4010-01-08-T4 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
43 | 00841911101406 | 4010-01-08-T3 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
44 | 00841911101390 | 4010-01-08-T1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
45 | 00841911101383 | 4010-01-08-S1 | HydroMARK Breast Biopsy Site Marker | NEU | Marker, Radiographic, Implantable | 2 | HydroMark | |
46 | 00841911101369 | MUK304 | Universal Biopsy Procedure Kit - Long | KNW | Instrument, Biopsy | 2 | Mammotome MR | |
47 | 00841911101352 | MUK303 | Universal Biopsy Procedure Kit - Short with Targeting Set | KNW | Instrument, Biopsy | 2 | Mammotome MR | |
48 | 00841911101345 | MUK302 | Universal Biopsy Procedure Kit - Long with Targeting Set | KNW | Instrument, Biopsy | 2 | Mammotome MR | |
49 | 00841911101338 | MUK301 | Universal Biopsy Procedure Kit - Short with Targeting Set | KNW | Instrument, Biopsy | 2 | Mammotome MR | |
50 | 00841911101321 | MRK304 | MR Biopsy Procedure Kit - Long with Targeting Set | KNW | Instrument, Biopsy | 2 | Mammotome MR |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00894912002135 | Smartdop 45 | Smartdop 45 | Bidirectional recording vascular Doppler. | Smartdop 45 | KOVEN TECHNOLOGY, INC. |
2 | EAMITRI20700 | TRI2070 | TRI2070 | The Wi-3 Arm is used to fix the outer (white) HAL-RAR sleeve in place to enhance The Wi-3 Arm is used to fix the outer (white) HAL-RAR sleeve in place to enhance gradual opening of the RAR window when mucopexy is performed, allowing the surgeon, the nurse or any assistant to comfortably hold the system in position.The Wi-3 HAL-RAR System (HAL - Hemorrhoidal Artery Ligation, RAR - Recto Anal Repair) is a Bluetooth-enabled, pulsed Doppler, ultrasound system intended to be used for detecting hemorrhoidal arteries, to manually ligate these arteries (HAL), and subsequently carry out a mucopexy of hemorrhoidal tissue prolapse (RAR) if necessary. | Wi-3 Arm | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH |
3 | EAMITRI20100 | TRI2010 | TRI2010 | Electronic unit for identifying the localised haemorrhoidal arteries by means of Electronic unit for identifying the localised haemorrhoidal arteries by means of acoustic signals. Part of the Wi-3 HAL-RAR System.The Wi-3 HAL-RAR System (HAL - Hemorrhoidal Artery Ligation, RAR - Recto Anal Repair) is a Bluetooth-enabled, pulsed Doppler, ultrasound system intended to be used for detecting hemorrhoidal arteries, to manually ligate these arteries (HAL), and subsequently carry out a mucopexy of hemorrhoidal tissue prolapse (RAR) if necessary. | Wi-3 HAL-RAR Unit | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH |
4 | EAMIRAR20810 | RAR2081 | RAR2081 | RAR Flexi Probe | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH | |
5 | EAMIRAR20110 | RAR 2011 | RAR 2011 | A.M.I. Recto Anal Repair Probe | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH | |
6 | EAMIAHH0010 | AHH 001 | AHH 001 | Handle for the HAL/RAR probes. | A.M.I. HAL Handle | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH |
7 | EAMIAHE2030 | AHE 203 | AHE 203 | Electronic unit for identifying the localised haemorrhoidal arteries by means of Electronic unit for identifying the localised haemorrhoidal arteries by means of acoustic signals. Part of the A.M.I. HAL/RAR System.The A.M.I. HAL-II Electronic System is a Doppler-based device. It is powered by a DC voltage source (rechargeable batteries or 12 V adapter). The A.M.I. HAL-II Electronic System generates electrical signals, calculates differences between the wavelength of outgoing and reflected electrical signals, and generates an acoustic Doppler signal.Together with auxiliary A.M.I. devices (A.M.I. HAL Handle, Probe and Sleeve) the A.M.I. HAL-II Electronic System serves for the detection of haemorrhoidal arteries and enables manual ligation of detected arteries, as well as mucopexy of prolapsing haemorrhoidal mucosa. | A.M.I. HAL-II Electronic System | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH |
8 | EAMIAHA0030 | AHA 003 | AHA 003 | A.M.I. HAL-II Adaptor USA | AMI AGENCY FOR MEDICAL INNOVATIONS GMBH | |
9 | 00885554034882 | 72204325 | 72204325 | HAT-TRICK MTP UNILATERAL PROC PACK | HAT-TRICK | SMITH & NEPHEW, INC. |
10 | 00884838114470 | 795186 | Software Version 6.X | Affiniti 70C Diagnostic Ultrasound System | PHILIPS ULTRASOUND, INC. | |
11 | 00884838114463 | 795185 | Software Version 6.X | Affiniti 70W Diagnostic Ultrasound System | PHILIPS ULTRASOUND, INC. | |
12 | 00884838114456 | 795187 | Software Version 6.X | Affiniti 70 Diagnostic Ultrasound System | PHILIPS ULTRASOUND, INC. | |
13 | 00884838113961 | 795125 | Software Version 9.x | EPIQ Elite Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
14 | 00884838113947 | 795123 | Software version 4.X | Lumify Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
15 | 00884838113930 | 795123 | Software version 3.x | Lumify Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
16 | 00884838113923 | 795122 | Software Version 9.x | EPIQ CVx Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
17 | 00884838113916 | 795122 | Software version 7.x | EPIQ CVx Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
18 | 00884838113909 | 795121 | Software version 9.X | Affiniti 30 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
19 | 00884838113893 | 795121 | Software version 7.x | Affiniti 30 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
20 | 00884838113886 | 795120 | Software Version 9.X | EPIQ 5 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
21 | 00884838113862 | 795119 | Software version 9.X | Affiniti 70 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
22 | 00884838113855 | 795119 | Software version 7.x | Affiniti 70 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
23 | 00884838113848 | 795118 | 9.X | Affiniti 50 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
24 | 00884838113831 | 795118 | Software Version 7.X | Affiniti 50 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
25 | 00884838113824 | 795117 | Software Version 9.X | EPIQ 7 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
26 | 00884838113800 | 795116 | Software version 3.X | Sparq Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
27 | 00884838113794 | 795116 | Software version 2.X | Sparq Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
28 | 00884838113787 | 795114 | Software version 5.X | CX50 Ultrasound Circular Edition | PHILIPS ULTRASOUND, INC. | |
29 | 00884838111004 | 795258 | Software version 6.X | EPIQ Elite W Diagnostic Ultrasound System | PHILIPS ULTRASOUND, INC. | |
30 | 00884838109971 | 795125 | To support the 7.x software version | EPIQ Elite Diamond Select Ultrasound | PHILIPS ULTRASOUND, INC. | |
31 | 00884838108479 | 795123 | Lumify Diamond Select | PHILIPS ULTRASOUND, INC. | ||
32 | 00884838108462 | 795216 | Lumify | PHILIPS ULTRASOUND, INC. | ||
33 | 00884838108455 | 795005 | Lumify System | PHILIPS ULTRASOUND, INC. | ||
34 | 00884838108448 | 795007 | Lumify Rugged System Bundle | PHILIPS ULTRASOUND, INC. | ||
35 | 00884838107748 | 795125 | EPIQ Elite Diamond Select Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
36 | 00884838107724 | 453561998453 | Lumify Power Module | PHILIPS ULTRASOUND, INC. | ||
37 | 00884838107540 | 795234 | EPIQ Elite Diagnostic Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
38 | 00884838107533 | 795232 | EPIQ CVxi Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
39 | 00884838107526 | 795231 | EPIQ CVx Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
40 | 00884838107519 | 795206 | EPIQ 5W Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
41 | 00884838107502 | 795204 | EPIQ 5 Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
42 | 00884838107489 | 795202 | EPIQ 7W Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
43 | 00884838107472 | 795122 | 9.0 and 9.0.x | EPIQ CVX Diamond Select | PHILIPS ULTRASOUND, INC. | |
44 | 00884838107465 | 795120 | EPIQ 5 Diamond Select Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
45 | 00884838107458 | 795117 | EPIQ 7 Diamond Select Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
46 | 00884838107441 | 795200 | EPIQ 7 Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
47 | 00884838107137 | 989606714631 | CX Cart Diamond Select | PHILIPS ULTRASOUND, INC. | ||
48 | 00884838106628 | 795218 | Affiniti 30 Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
49 | 00884838106611 | 795210 | Affiniti 70 Ultrasound System | PHILIPS ULTRASOUND, INC. | ||
50 | 00884838106604 | 795208 | Affiniti 50 Ultrasound System | PHILIPS ULTRASOUND, INC. |