Other products from "HOLOGIC, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 15420045515031 2050-0104 2050-0104 MWP Cabinet, x-ray system 2 FAXITRON PATH
2 15420045514089 R15 R15 GDF GUIDE, NEEDLE, SURGICAL 1 PERL
3 15420045506909 Discovery C KGI Densitometer, bone 2 Discovey C
4 15420045504110 ATEC Sapphire 200 KNW INSTRUMENT, BIOPSY 2 ATEC Sapphire 200
5 15420045510333 50-250XL HIH HYSTEROSCOPE (AND ACCESSORIES) 2 MYOSURE XL HYSTEROSCOPY SET
6 15420045514294 V5 NSV5US-001 MNB Device, thermal ablation, endometrial 3 NovaSure
7 25420045510330 50-250XL HIH HYSTEROSCOPE (AND ACCESSORIES) 2 MYOSURE XL HYSTEROSCOPY SET
8 25420045514307 V5 NSV5KITUS-001 MNB Device, thermal ablation, endometrial 3 NovaSure
9 25420045505107 40-902 40-902 HIH HYSTEROSCOPE (AND ACCESSORIES) 2 MyoSure Tissue Removal Device
10 15420045514836 PATHVISION 23x29 PATHVISION23X29 MWP Cabinet, x-ray system 2 FAXITRON PATH
11 15420045514300 V5 NSV5KITUS-001 MNB Device, thermal ablation, endometrial 3 NovaSure
12 15420045512924 INTERNAL CONTROL-B, 960T, IVD PRD-06234 JJH CLINICAL SAMPLE CONCENTRATOR 1 Panther Fusion
13 15420045512917 EXTRACTION REAGENTS-B, 960T, IVD PRD-06232 JJH CLINICAL SAMPLE CONCENTRATOR 1 Panther Fusion
14 15420045510906 GBS CTRLS KIT, PANTHER FUSION, IVD PRD-04485 NJR Nucleic acid amplification assay system, group b streptococcus, direct specimen test 1 Panther Fusion
15 15420045510890 GBS KIT, 96T, IVD PRD-04484 NJR Nucleic acid amplification assay system, group b streptococcus, direct specimen test 1 Panther Fusion
16 15420045510470 INTERNAL CONTROL-X, 960T, IVD PRD-04476 NJR Nucleic acid amplification assay system, group b streptococcus, direct specimen test 1 Panther Fusion
17 15420045510463 EXTRACTION REAGENT-X, 960T, IVD PRD-04477 NJR Nucleic acid amplification assay system, group b streptococcus, direct specimen test 1 Panther Fusion
18 15420045509641 System Software InSight FD OXO Image-intensified fluoroscopic x-ray system, mobile 2 Flouroscan InSight
19 15420045509375 CLASS I CONTROL - C. ALBICANS PRD-04521 JJX Single (specified) analyte controls (assayed and unassayed) 1 aptima
20 15420045507937 20-401ML 20-401ML NWW Hysteroscope accessories Myosure Manual Tissue Removal Device
21 15420045505230 B90003 B90003 JAQ System, applicator, radionuclide, remote-controlled 2 4.0-5.0 CM CT LUMEN MARKER SET
22 15420045505193 B11245 B11245 JAQ System, applicator, radionuclide, remote-controlled 2 4-5 CM CONTURAFLEX MLB CATHETER w/TRI INTRODUCER
23 15420045505094 50-501XL 50-501XL HIH HYSTEROSCOPE (AND ACCESSORIES) MyoSure Tissue Removal Device
24 15420045505087 50-401XL 50-401XL HIH HYSTEROSCOPE (AND ACCESSORIES) 2 MyoSure Tissue Removal Device
25 15420045505070 30-401LITE 30-401LITE HIH HYSTEROSCOPE (AND ACCESSORIES) MyoSure Tissue Removal Device
26 15420045505001 919007-01 919007-01 JAQ System, applicator, radionuclide, remote-controlled Mammosite Variable 4-5 cm Applicator Tray
27 15420045504998 EVIVA_1213-20 EVIVA_1213-20 KNW INSTRUMENT, BIOPSY EVIVA_1213-20
28 15420045504950 EVIVA_0910-20 EVIVA_0910-20 KNW INSTRUMENT, BIOPSY EVIVA_0910-20
29 15420045504813 10-401 10-401 HIH HYSTEROSCOPE (AND ACCESSORIES) MyoSure Tissue Removal Device
30 15420045501140 2000 NS2000US MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL NovaSure
31 15420045501133 2007 NS2007US MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL NovaSure SureSound
32 15420045501126 2013 NS2013KITUS MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL NovaSure SureSound
33 15420045501119 2013 NS2013US MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL NovaSure
34 15420045501065 Cervista HTA System Computer MAQ KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS 3 Cervista HTA System
35 15420045500969 Cervista HTA System MAQ KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS 3 Cervista HTA System
36 15420045500952 Cervista HTA System MAQ KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS 3 Cervista HTA System
37 15420045500860 NovaSure Controller MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL 3 NovaSure
38 15420045500853 NovaSure Controller MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL 3 NovaSure
39 15420045512474 GENIUS AI DETECTION SOFTWARE OTE Digital breast tomosynthesis 3 GENIUS AI DETECTION
40 25420045510064 FILTER, THINPREP UROCYTE 100 PACK   70472-001 KET FILTERS, CELL COLLECTION, TISSUE PROCESSING ThinPrep
41 25420045510057 THINPREP SLIDES UROCYTE, 100 pk 70471-001 KEW SLIDES, MICROSCOPE ThinPrep
42 25420045509990 THINPREP MICROSCOPE, ARCLESS, 72pk 70126-002 KEW SLIDES, MICROSCOPE ThinPrep
43 25420045509679 NON-GYN Slides 70372-001 KEW SLIDES, MICROSCOPE ThinPrep
44 25420045509662 NON-GYN Filters, 100 pack 70205-001 KET FILTERS, CELL COLLECTION, TISSUE PROCESSING ThinPrep
45 25420045508467 UroCyte Vial 70473-001  LEA PRESERVATIVE, CYTOLOGICAL 1 ThinPrep
46 25420045505039 819001 819001 JAQ System, applicator, radionuclide, remote-controlled 2 Neucletron HDR Afterloader Connectors wObturators
47 15420045514775 PRESERVCYT VIAL PRD-07129 LEA PRESERVATIVE, CYTOLOGICAL 1 ThinPrep
48 15420045514621 UroCyte Vial ASY-15509 LEA PRESERVATIVE, CYTOLOGICAL 1 ThinPrep
49 15420045514614 CytoLyt Cup PRD-07065 LEA PRESERVATIVE, CYTOLOGICAL 1 ThinPrep
50 15420045514607 CytoLyt Tube PRD-07064 LEA PRESERVATIVE, CYTOLOGICAL 1 ThinPrep
Other products with the same Product Code "OCC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Amplification Tray LUMINEX CORPORATION
2 00840487101667 20-009-024 20-009-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Extraction Tray LUMINEX CORPORATION
3 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge LUMINEX CORPORATION
4 00840487100486 I025C0197 I025C0197 The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected ofrespiratory tract infections xTAG® RVP FAST (Respiratory Viral Panel Fast) LUMINEX MOLECULAR DIAGNOSTICS, INC
5 00840487100462 I019C0111 I019C0111 The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected of respiratory tract infections. xTAG® RVP (Respiratory Viral Panel) LUMINEX MOLECULAR DIAGNOSTICS, INC
6 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
7 00840487100158 50-10020 The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualit The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection and differentiation of influenza A virus, influenza B virus, and respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal swabs (NPS) specimens from patients with signs and symptoms of respiratory tract infection in conjunction with clinical and laboratory findings. ARIES® Flu A/B & RSV Assay LUMINEX CORPORATION
8 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
9 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
10 00815381020147 RFIT-ASY-0120 RFIT-ASY-0120 IVD reagent kit containing 30 tests. FilmArray® Respiratory Panel (RP) EZ BIOFIRE DIAGNOSTICS, LLC
11 00815381020079 RFIT-ASY-0125 RFIT-ASY-0125 IVD reagent kit containing 6 tests. FilmArray® Respiratory Panel (RP) BIOFIRE DIAGNOSTICS, LLC
12 00815381020062 RFIT-ASY-0124 RFIT-ASY-0124 IVD reagent kit containing 30 tests. FilmArray® Respiratory Panel (RP) BIOFIRE DIAGNOSTICS, LLC
13 B540FAB1100CWC0 FAB1100CW-C FAB1100CW-1 The Accula™ Flu A / B Control Kit is intended for in vitro diagnostic use in qua The Accula™ Flu A / B Control Kit is intended for in vitro diagnostic use in qualitycontrol testing with the Accula™ Flu A / B Test. Accula Flu A / B Control Kit MESA BIOTECH, INC.
14 B540FAB1100CW0 FAB1100CW FAB1100CW The Accula™ Flu A / B Test performed on the Accula Dock is a molecular in vitro The Accula™ Flu A / B Test performed on the Accula Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Accula Flu A / B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Accula Flu A / B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus. Accula Flu A / B Test MESA BIOTECH, INC.
15 B540D20010 D2001 D2001 The Programming Cassette is an accessory to the Accula Dock and facilitates repr The Programming Cassette is an accessory to the Accula Dock and facilitates reprogramming of the Dock’s embedded firmware. When firmware updates are needed, the firmware will be stored onto Programming Cassettes and sent to end users, who will load the Programming Cassette into their Dock and re-program its firmware Accula Programming Cassette MESA BIOTECH, INC.
16 B540D20000 D2000 D2000 The Accula Dock is an electronic module which executes in vitro diagnostic tests The Accula Dock is an electronic module which executes in vitro diagnostic tests on compatible Test Cassettes. It consists of anelectro-mechanical interface to a single Test Cassette. The Dock contains all electrical systems, controls and logic necessary toorchestrate in-vitro diagnostic tests within the inserted Test Cassette. Accula Dock MESA BIOTECH, INC.
17 B54010400 1040 1040 The Silaris™ RSV Test performed on the Silaris™ Dock is a molecular in vitro dia The Silaris™ RSV Test performed on the Silaris™ Dock is a molecular in vitro diagnostic test utilizing polymerase chainreaction (PCR) and lateral flow technologies for the qualitative, visual detection of respiratory syncytial virus (RSV) viral RNA.The Silaris RSV Test uses a nasal swab specimen collected from patients with signs and symptoms of respiratory infection.The Silaris RSV Test is intended as an aid in the diagnosis of RSV infection in children and adults in conjunction with clinicaland epidemiological risk factors. Silaris RSV Supplemental Pack MESA BIOTECH, INC.
18 B54010350 1035 1035 The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Silaris Influenza A&B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Silaris Influenza A&B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus. Sialris Influenza A&B Supplemental Pack MESA BIOTECH, INC.
19 B54010290 1029 1029 The Silaris RSV Control Kit is intended for in vitro diagnostic use in quality c The Silaris RSV Control Kit is intended for in vitro diagnostic use in quality control testing with the Silaris RSV Test Silaris RSV Control Kit MESA BIOTECH, INC.
20 B54010280 1028 1028 The Silaris Starter Pack contains two (2) Silaris Influenza A&B kits and one (1) The Silaris Starter Pack contains two (2) Silaris Influenza A&B kits and one (1) Silaris Dock for the purposes of starting up a clinical location. SilarisTM Influenza A&B Starter Pack MESA BIOTECH, INC.
21 B54010270 1027 1027 The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Silaris Influenza A&B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Silaris Influenza A&B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus. Silaris Influenza A&B Test MESA BIOTECH, INC.
22 B54010240 1024 1024 The Silaris™ Influenza A&B Control Kit is intended for in vitro diagnostic use i The Silaris™ Influenza A&B Control Kit is intended for in vitro diagnostic use in qualitycontrol testing with the Silaris™ Influenza A&B Test. Silaris Influenza A&B Control Kit MESA BIOTECH, INC.
23 30014613336143 M306 M306 Solana RSV/hMPB Assay Solana DIAGNOSTIC HYBRIDS, INC.
24 30014613336068 M300 M300 Solana Infulenza A+B Assay Solana DIAGNOSTIC HYBRIDS, INC.
25 30014613311133 Adenovirus Assay M113 Lyra Adenovirus Assay Lyra QUIDEL CORPORATION
26 30014613311034 M103 M103 Lyra RSV+HMPV Assay Lyra DIAGNOSTIC HYBRIDS, INC.
27 30014613311003 M100 M100 Lyra FLU A+B Assay Lyra DIAGNOSTIC HYBRIDS, INC.
28 20816101025552 MOL2660 Simplexa™ Flu A/B & RSV Positive Control Pack DIASORIN MOLECULAR LLC
29 20816101025545 MOL2650 Simplexa™ Flu A/B & RSV Direct DIASORIN MOLECULAR LLC
30 20816101025538 MOL2600 Simplexa™ Flu A/B & RSV DIASORIN MOLECULAR LLC
31 15420045509320 AMR CTRLS, PANTHER FUSION, IVD PRD-04338 PANTHER FUSION HOLOGIC, INC.
32 15420045509313 FLU A B RSV CTRLS, PANTHER FUSION, IVD PRD-04336 PANTHER FUSION HOLOGIC, INC.
33 15420045509290 AMR KIT, PANTHER FUSION, 96T, IVD PRD-04330 PANTHER FUSION HOLOGIC, INC.
34 15420045509283 FLU A B RSV, PANTHER FUSION, 96T, IVD PRD-04328 PANTHER FUSION HOLOGIC, INC.
35 15420045509276 OIL KIT, PANTHER FUSION, 1920T, IVD PRD-04335 PANTHER FUSION HOLOGIC, INC.
36 15420045509269 ELUTION KIT, PANTHER FUSION, 2400T, IVD PRD-04334 PANTHER FUSION HOLOGIC, INC.
37 15420045509252 RECON-1 KIT, PANTHER FUSION, 1920T, IVD PRD-04333 PANTHER FUSION HOLOGIC, INC.
38 15420045509238 SPECIMEN LYSIS TUBES, IVD PRD-04339 PANTHER FUSION HOLOGIC, INC.
39 15420045509221 INTERNAL CONTROL-S, 960T, IVD PRD-04332 PANTHER FUSION HOLOGIC, INC.
40 15420045509214 EXTRACTION REAGENT-S, 960T, IVD PRD-04331 PANTHER FUSION HOLOGIC, INC.
41 15420045506381 PROADENO+ KIT, 100 REACTIONS 303675 PRODESSE HOLOGIC, INC.
42 15420045506343 PROFLU+ ASSAY KIT, 1,500 REACTIONS 303123 PRODESSE HOLOGIC, INC.
43 15420045506336 PROFLU+ ASSAY KIT, 2,000 REACTIONS 303121 PRODESSE HOLOGIC, INC.
44 15420045506329 PRODESSE PROFLU+ ASSAY 303111 PRODESSE HOLOGIC, INC.
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46 07613336129685 08085463001 08085463001 cobas® Liat® Influenza A/B Script ROCHE MOLECULAR SYSTEMS, INC.
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