No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00884999002180 | 02J27-095 | 02J27-095 | UroVysion Bladder Cancer Kit | NSD | Test, fluorescence in situ hybridization (fish), for bladder cancer detection an Test, fluorescence in situ hybridization (fish), for bladder cancer detection and monitoring for recurrence | 3 | UroVysion |
2 | 00884999002142 | 02J27-025 | 02J27-025 | UroVysion Bladder Cancer Kit | NSD | Test, fluorescence in situ hybridization (fish), for bladder cancer detection an Test, fluorescence in situ hybridization (fish), for bladder cancer detection and monitoring for recurrence | 3 | UroVysion |
3 | 00884999002128 | 02J27-011 | 02J27-011 | ProbeChek UroVysion Bladder Cancer Kit Control Slides | OYU | Dna-probe kit, human chromosome | 2 | UroVysion |
4 | 00884999031357 | 8L49-030 | 8L49-30 | DNA Amp Check | PPM | General purpose reagent | 1 | Abbott |
5 | 00884999039278 | 4J94-23 | 4J94-23 | ViroSeq HIV-1 Genotyping Software v3.0 & Algorithm Advisor | NHS | Assay, genotype, hiv drug resistance, in vitro | 2 | ViroSeq |
6 | 00884999007475 | 4J94-93 | 4J94-93 | ViroSeq HIV-1 Genotyping System v2.0 | NHS | Assay, genotype, hiv drug resistance, in vitro | 2 | ViroSeq |
7 | 00884999007468 | 4J94-92 | 4J94-92 | Sequencing Consumables Kit | PPM | General purpose reagent | 1 | ViroSeq |
8 | 00884999007420 | 4J94-73 | 4J94-73 | PCR Cleanup Kit | PPM | General purpose reagent | 1 | ViroSeq |
9 | 00884999049130 | 09N77-055 | 09N77-055 | Abbott Universal Collection Kit | QJR | Reagents, 2019-novel coronavirus nucleic acid | RealTime | |
10 | 00884999049109 | 09N77-095 | 09N77-095 | Abbott RealTime SARS-CoV-2 Amplification Reagent Kit | QJR | Reagents, 2019-novel coronavirus nucleic acid | RealTime | |
11 | 00884999049086 | 09N77-085 | 09N77-085 | Abbott RealTime SARS-CoV-2 Control Kit | QJR | Reagents, 2019-novel coronavirus nucleic acid | RealTime | |
12 | 00884999049055 | 09N77-010 | 09N77-010 | Abbott RealTime SARS-CoV-2 Application CD-ROM | QJR | Reagents, 2019-novel coronavirus nucleic acid | RealTime | |
13 | 00884999048478 | 02J11-057 | 02J11-057 | VP 2000 System Software v2.1 with Protocols USB | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
14 | 00884999048065 | 06L83-008 | 06L83-008 | Abbott RealTime HIV-1 m2000 System Combined Application CD-ROM | MZF | Test, HIV detection | 2 | RealTime |
15 | 00884999047792 | 08N90-006 | 08N90-006 | Abbott RealTime IDH1m2000rt Application CD-ROM | OWD | Somatic gene mutation detection system | 3 | RealTime |
16 | 00884999047341 | 08N90-080 | 08N90-080 | Abbott RealTime IDH1 Control Kit | OWD | Somatic gene mutation detection system | 3 | RealTime |
17 | 00884999047310 | 02J11-065 | 02J11-065 | VIP 2000 Upgrade Kit | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
18 | 00884999047297 | 09N21-002 | 09N21-002 | Abbott RealTime CMV m2000 System Combined Application CD-ROM | PAB | Cytomegalovirus (cmv) dna quantitative assay | 3 | RealTime |
19 | 00884999047051 | 08N82-080 | Abbott RealTime IDH2 Control Kit | OWD | Somatic gene mutation detection system | 3 | RealTime | |
20 | 00884999047044 | 08N82-090 | 08N82-090 | Abbott RealTime IDH2 Amplification Reagent Kit | OWD | Somatic gene mutation detection system | 3 | RealTime |
21 | 00884999047037 | 08N82-001 | 08N82-001 | Abbott RealTime IDH2 m2000rt Application CD-ROM | OWD | Somatic gene mutation detection system | 3 | RealTime |
22 | 00884999046603 | 03L78-061 | 03L78-061 | Abbott Proteinase K Recombinant, PCR Grade | PAB | Cytomegalovirus (cmv) dna quantitative assay | 3 | RealTime |
23 | 00884999046528 | 9K12-04 | 9K12-04 | multi-Collect Specimen Collection Kit | LSL,LIO,MKZ | DNA-REAGENTS, NEISSERIA,DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPL DNA-REAGENTS, NEISSERIA,DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA | Multi-Collect | |
24 | 00884999046511 | 9K12-03 | 9K12-03 | multi-Collect Specimen Collection Specimen Collection Kit | MKZ,LIO,LSL | DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA,DEVICE, SPECIMEN COLLECTION,DNA DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA,DEVICE, SPECIMEN COLLECTION,DNA-REAGENTS, NEISSERIA | Multi-Collect | |
25 | 00884999046153 | 02J11-042 | 02J11-042 | VIP 2000 Upgrade 250 mL Basin Kit | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
26 | 00884999046146 | 02J11-041 | 02J11-041 | VIP 2000 Upgrade 150 mL Basin Kit | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
27 | 00884999046122 | 02J11-063 | 02J11-063 | VP 2000 Processor, 100V | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
28 | 00884999046115 | 02J11-062 | 02J11-062 | VP 2000 Processor, 117V | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
29 | 00884999046108 | 02J11-061 | 02J11-061 | VP 2000 Processor, 230V | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
30 | 00884999045798 | 09N21-090 | 09N21-090 | Abbott RealTime CMV Amplification Reagent Kit | PAB | Cytomegalovirus (cmv) dna quantitative assay | 3 | RealTime |
31 | 00884999045781 | 09N21-080 | 09N21-080 | Abbott RealTime CMV Control Kit | PAB | Cytomegalovirus (cmv) dna quantitative assay | 3 | RealTime |
32 | 00884999045774 | 09N21-070 | 09N21-070 | Abbott RealTime CMV Calibrator Kit | PAB | Cytomegalovirus (cmv) dna quantitative assay | 3 | RealTime |
33 | 00884999042704 | 06L83-007 | 06L83-007 | Abbott RealTime HIV-1 m2000 System Combined Application CD-ROM | MZF | Test, hiv detection | 2 | RealTime |
34 | 00884999042681 | 04N45-004 | 04N45-004 | Abbott RealTime HCV m2000 System Combined Application CD-ROM | MZP | ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS C RNA,HEPATITIS C VIRUS | 2 | RealTime |
35 | 00884999042667 | 02N43-004 | 02N43-004 | Abbott RealTime HBV m2000 System Combined Application CD-ROM | MKT | Hepatitis Viral B DNA Detection | 3 | RealTime |
36 | 00884999042513 | 08L21-002 | 08L21-002 | Abbott RealTime HCV Genotype II m2000 System Combined Application CD-ROM | OBF | Assay, genotyping, hepatitis c virus | 2 | RealTime |
37 | 00884999038462 | 2N40-91 | 2N40-91 | Abbott RealTime HBV Amplification Reagent Kit | MKT | Hepatitis Viral B DNA Detection | 3 | RealTime |
38 | 00884999038189 | 08N16-001 | 08N16-001 | VP 2000 Pretreatment Kit | OWE | Fluorescence in situ hybridization, anaplastic lymphoma kinase, gene rearrangement | 3 | VP2000 |
39 | 00884999037762 | 2N43-03 | 2N43-03 | Abbott RealTime HBV m2000 System Combined Application CD-ROM, Version 3.0 | MKT | Hepatitis Viral B DNA Detection | 3 | RealTime |
40 | 00884999037656 | 4N45-03 | 4N45-03 | Abbott RealTime HCV m2000 System Combined Application CD-ROM, Version 3.0 | MZP | ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS C RNA,HEPATITIS C VIRUS | 2 | RealTime |
41 | 00884999037595 | 03N27-51 | 03N27-51 | Abbott VP2000 Processor Operations Manual, Rev. D | KEY | STAINER, TISSUE, AUTOMATED | 1 | VP2000 |
42 | 00884999037472 | 06L87-02 | 06L87-02 | Uracil-N-Glycosylase (UNG) | MZP,LSL,OBF,MZF,MKZ | ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS C RNA,HEPATITIS C VIRUS,DNA-REAGENTS, NEISSERIA,Assay, genotyping, hepatitis c virus,Test, hiv detection,DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA | 1 | RealTime |
43 | 00884999037434 | 1N30-67 | 1N30-67 | Abbott RealTime HCV Including Uracil-N-Glycosylase (UNG) | MZP | ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS ASSAY,HYBRIDIZATION AND/OR NUCLEIC ACID AMPLIFICATION FOR DETECTION OF HEPATITIS C RNA,HEPATITIS C VIRUS | 2 | RealTime |
44 | 00884999037427 | 6L18-67 | 6L18-67 | Abbott RealTime HIV-1 Amplification Extended Use Including Uracil-N-Glycosylase (UNG) | MZF | Test, hiv detection | 2 | RealTime |
45 | 00884999037410 | 8L07-67 | 8L07-67 | Abbott RealTime CT/NG Amplification Reagent Extended Use Including Uracil-N-Glyc Abbott RealTime CT/NG Amplification Reagent Extended Use Including Uracil-N-Glycosylase (UNG) | LIO,MKZ,LSL | DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA,DNA DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA,DNA-REAGENTS, NEISSERIA | 1 | RealTime |
46 | 00884999037304 | 6L18-50 | 6L18-50 | Abbott RealTime HIV-1 Amplification Reagent Extended Use | MZF | Test, hiv detection | 2 | RealTime |
47 | 00884999037298 | 8L07-50 | 8L07-50 | Abbott RealTime CT/NG Amplification Reagent Extended Use with Pierceable Caps | LSL,LIO,MKZ | DNA-REAGENTS, NEISSERIA,DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPL DNA-REAGENTS, NEISSERIA,DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA | 1 | RealTime |
48 | 00884999037168 | 6L83-06 | 6L83-06 | Abbott RealTime HIV-1 m2000 System Combined Application CD-ROM, Version 6.0 | MZF | Test, hiv detection | 2 | RealTime |
49 | 00884999037113 | 06L98-05 | 06L98-05 | Abbott m2000 System Chlamydia trachomatis and Neisseria gonorrhoeae Application Abbott m2000 System Chlamydia trachomatis and Neisseria gonorrhoeae Application CD-ROM, Version 5.0 | LSL,LIO,MKZ | DNA-REAGENTS, NEISSERIA,DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPL DNA-REAGENTS, NEISSERIA,DEVICE, SPECIMEN COLLECTION,DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA | 1 | RealTime |
50 | 00884999036444 | 08L21-66 | 08L21-66 | Uracil-N-Glycosylase (UNG) for use in conjunction with Abbott RealTime HCV Genot Uracil-N-Glycosylase (UNG) for use in conjunction with Abbott RealTime HCV Genotype II Assay | OBF | Assay, genotyping, hepatitis c virus | 2 | RealTime |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 03573026559823 | 1.0 | Software used in combination with the THxIDTM- BRAF assay(used to identify patie Software used in combination with the THxIDTM- BRAF assay(used to identify patients with melanoma whose tumors harbor the BRAF V600E/K mutations) | THxID™ BRAF | BIOMERIEUX SA | |
2 | 03573026354909 | 410697 | 410697 | The THxID™ BRAF kit is an IVD real time PCR device intended for the qualitative The THxID™ BRAF kit is an IVD real time PCR device intended for the qualitative detection of the BRAF V600E and V600K mutations in human melanoma tissue | THxID™-BRAF | BIOMERIEUX SA |
3 | 00884999047792 | 08N90-006 | 08N90-006 | Abbott RealTime IDH1m2000rt Application CD-ROM | RealTime | ABBOTT MOLECULAR INC. |
4 | 00884999047358 | 08N90-090 | 08N90-090 | Abbott RealTime IDH1 Amplification Reagent Kit | RealTime | ABBOTT MOLECULAR INC. |
5 | 00884999047341 | 08N90-080 | 08N90-080 | Abbott RealTime IDH1 Control Kit | RealTime | ABBOTT MOLECULAR INC. |
6 | 00884999047051 | 08N82-080 | Abbott RealTime IDH2 Control Kit | RealTime | ABBOTT MOLECULAR INC. | |
7 | 00884999047044 | 08N82-090 | 08N82-090 | Abbott RealTime IDH2 Amplification Reagent Kit | RealTime | ABBOTT MOLECULAR INC. |
8 | 00884999047037 | 08N82-001 | 08N82-001 | Abbott RealTime IDH2 m2000rt Application CD-ROM | RealTime | ABBOTT MOLECULAR INC. |
9 | 00875197005592 | 7258321190 | 07258321190 | cobas® EZH2 Mutation Test | ROCHE MOLECULAR SYSTEMS, INC. | |
10 | 00875197005448 | 2.0 | 07248563190 | cobas® EGFR Mutation Test v2 | ROCHE MOLECULAR SYSTEMS, INC. | |
11 | 00875197004229 | 06471463190 | 06471463190 | cobas® EGFR Mutation Test | ROCHE MOLECULAR SYSTEMS, INC. | |
12 | 00875197004199 | 1.0 | 05852170190 | cobas® KRAS Mutation Test | ROCHE MOLECULAR SYSTEMS, INC. | |
13 | 00875197004137 | 05985579190 | 05985579190 | cobas® 4800 BRAF V600 Mutation Test | ROCHE MOLECULAR SYSTEMS, INC. | |
14 | 00875197004120 | 05985536190 | 05985536190 | cobas® DNA Sample Preparation Kit | ROCHE MOLECULAR SYSTEMS, INC. | |
15 | 00850052003739 | 850052003739 | K4120361 | The LeukoStrat CDx FLT3 Mutation Assay is a PCR-based in vitro diagnostic test d The LeukoStrat CDx FLT3 Mutation Assay is a PCR-based in vitro diagnostic test designed to detect internal tandem duplication (ITD) and tyrosine kinase domain (TKD) mutations D835 and I836 in the FLT3 gene in genomic DNA extracted from mononuclear cells obtained from peripheral blood or bone marrow aspirates of patients diagnosed with acute myelogenous leukemia (AML). | LeukoStrat | INVIVOSCRIBE, INC. |
16 | 00850052003685 | 850052003685 | K4120221 | The LeukoStrat CDx FLT3 Mutation Assay targets regions of the FLT3 gene to ident The LeukoStrat CDx FLT3 Mutation Assay targets regions of the FLT3 gene to identify internal tandem duplication (ITD) mutations and tyrosine kinase domain (TKD) mutations, such as the D835 and I836 mutations. The LeukoStrat CDx FLT3 Mutation Assay includes reagents, equipment, software and procedures for isolating mononuclear cells and extracting DNA from patient specimens to determine if FLT3 mutations are present. DNA is amplified via PCR, TKD amplicon is enzymatically digested, and the amplicons are detected via capillary electrophoresis. | LeukoStrat | INVIVOSCRIBE, INC. |
17 | 00054749005529 | 04P75-03 | i-STAT 1 Wireless | i-STAT | ABBOTT POINT OF CARE INC. | |
18 | 00054749005222 | 03P75-90 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
19 | 00054749005215 | 03P75-89 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
20 | 00054749005208 | 03P75-88 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
21 | 00054749005192 | 03P75-87 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
22 | 00054749005185 | 03P75-86 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
23 | 00054749005178 | 03P75-85 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
24 | 00054749005161 | 03P75-84 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
25 | 00054749005154 | 03P75-83 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
26 | 00054749005147 | 03P75-82 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
27 | 00054749005123 | 03P75-81 | i-Stat 1 Wireless Analyzer | i-STAT | ABBOTT POINT OF CARE INC. | |
28 | 00054749005093 | 03P75-07 | i-STAT 1 Wireless | i-STAT | ABBOTT POINT OF CARE INC. | |
29 | 10054749005519 | 09P31-26 | Cartridge, Chem8+ | i-STAT | ABBOTT POINT OF CARE INC. | |
30 | 10054749005502 | 03P85-51 | Cartridge, CG4+ | i-STAT | ABBOTT POINT OF CARE INC. | |
31 | 04053228043560 | 2 | 874721 | The therascreen FGFR RGQ RT-PCR Kit is a real-time, reverse transcription PCR te The therascreen FGFR RGQ RT-PCR Kit is a real-time, reverse transcription PCR test for the qualitative detection of two point mutations in exon 7 [p.R248C (c.742C>T), p.S249C (c.746C>G)], two point mutations in exon 10 [p.G370C (c.1108G>T) and p.Y373C (c.1118A>G)] and two fusions (FGFR3-TACC3v1 and FGFR3-TACC3v3) in the fibroblast growth factor receptor 3 (FGFR3) gene in RNA samples derived from formalin-fixed paraffin-embedded (FFPE) urothelial tumor tissue. The test is indicated for use as an aid in identifying patients with cases of urothelial cancer (UC) which harbor these alterations and are therefore eligible for treatment with BALVERSA™ (erdafitinib).Specimens are processed using the RNeasy DSP FFPE Kit for manual sample preparation followed by reverse transcription and then automated amplification and detection on the Rotor-Gene Q MDx (US) instrument. | therascreen® FGFR RGQ RT-PCR Kit | QIAGEN GMBH |
32 | 04053228035725 | 1 | 874821 | The therascreen BRAF V600E RGQ PCR Kit is a real-time PCR test for the qualitati The therascreen BRAF V600E RGQ PCR Kit is a real-time PCR test for the qualitative detection of V600E mutations in the BRAF gene using genomic DNA extracted from formalin-fixed paraffin-embedded (FFPE) human colorectal cancer (CRC) tumor tissue. The therascreen BRAF V600E RGQ PCR Kit is an in vitro diagnostic device intended to be used as an aid in selecting patients with metastatic colorectal cancer (mCRC) whose tumors carry the BRAF V600E mutation for treatment with BRAFTOVI (encorafenib) in combination with cetuximab. The therascreen BRAF V600E RGQ PCR Kit is for use on the Rotor-Gene Q MDx (US)instrument. The therascreen BRAF V600E RGQ PCR Kit is intended for in vitro diagnostic use. | therascreen® BRAF RGQ PCR Kit | QIAGEN GMBH |
33 | 04053228034223 | V1 | 873121 | The therascreen PIK3CA RGQ PCR Kit is a real-time qualitative PCR test for the d The therascreen PIK3CA RGQ PCR Kit is a real-time qualitative PCR test for the detection of 11 mutations in the phosphatidylinositol 3-kinase catalytic subunit alpha (PIK3CA) gene (Exon 7: C420R; Exon 9: E542K, E545A, E545D [1635G>T only], E545G, E545K, Q546E, Q546R; and Exon 20: H1047L, H1047R, H1047Y) using genomic DNA (gDNA) extracted from formalin-fixed, paraffin-embedded (FFPE) breast tumor tissue or circulating tumor DNA (ctDNA) from plasma derived from K2EDTA anticoagulated peripheral whole blood taken from patients with breast cancer. The test is intended to aid clinicians in identifying breast cancer patients who may be eligible for treatment with PIQRAY® (alpelisib) based on a PIK3CA Mutation Detected result. Patients whose FFPE tissue or plasma specimen produces a positive therascreen PIK3CA RGQ PCR Kit test result for the presence of one or more PIK3CA mutations are eligible for treatment with PIQRAY (alpelisib). Patients whose plasma specimen produces a negative result using this test should be reflexed to testing with FFPE tumor tissue for the presence of PIK3CA mutations. FFPE tumor specimens are processed using the QIAamp DSP DNA FFPE Tissue Kit for manual sample preparation. K2EDTA anticoagulated whole peripheral venous blood plasma specimens are processed using the QIAamp DSP Circulating Nucleic Acid Kit for manual sample preparation. For both specimen types, the Rotor-Gene Q (RGQ) MDx (US) instrument is used for automated amplification and detection. The Kit is to be used by trained personnel in a professional laboratory environment. | therascreen® PIK3CA RGQ PCR Kit | QIAGEN GMBH |
34 | 04053228034094 | V1 | 874721 | The therascreen FGFR RGQ RT-PCR Kit is a real-time, reverse transcription PCR te The therascreen FGFR RGQ RT-PCR Kit is a real-time, reverse transcription PCR test for the qualitative detection of two point mutations in exon 7 [p.R248C (c.742C>T), p.S249C (c.746C>G)], two point mutations in exon 10 [p.G370C (c.1108G>T) and p.Y373C (c.1118A>G)] and two fusions (FGFR3:TACC3v1 and FGFR3:TACC3v3) in the fibroblast growth factor receptor 3 (FGFR3) gene in RNA samples derived from formalin-fixed paraffin-embedded (FFPE) urothelial tumor tissue. The test is indicated for use as an aid in identifying patients with cases of urothelial cancer (UC) which harbor these alterations and are therefore eligible for treatment with BALVERSA™ (erdafitinib).Specimens are processed using the RNeasy DSP FFPE Kit for manual sample preparation followed by reverse transcription and then automated amplification and detection on the Rotor-Gene Q MDx (US) instrument. | therascreen® FGFR RGQ RT-PCR Kit | QIAGEN GMBH |
35 | 04053228002062 | 1 | 870121 | therascreen® EGFR RGQ PCR Kit | QIAGEN GMBH | |
36 | 04053228002048 | 1 | 870021 | therascreen® KRAS RGQ PCR Kit | QIAGEN GMBH |