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Intraspinal Catheter Kit
Medos International Sàrl
60-2918US
Not in Commercial Distribution
- 10886704028444 ()
602918US
- Spinal port/catheter
Pump Catheter
Medos International Sàrl
60-2914US
Not in Commercial Distribution
- 10886704028420 ()
602914US
- Spinal port/catheter
Intraspinal Catheter Connector with Strain Relief Sleeve
Medos International Sàrl
70029US
Not in Commercial Distribution
- 10886704072560 ()
70029US
- Spinal port/catheter
Intraspinal Catheter Kit A.1 SureStream Catheter;19-gauge;with Guide Wire B.1 Catheter-threading guide C.1 SureStream Connector;titanium D. Anchors 1 each of 4 styles
Medos International Sàrl
70020US
Not in Commercial Distribution
- 10886704072553 ()
70020US
- Spinal port/catheter
Intraspinal Catheter Connector with Strain Relief Sleeve
Medos International Sàrl
60-2950US
Not in Commercial Distribution
- 10886704067764 ()
602950US
- Spinal port/catheter
Control Unit Includes: Control Unit;Hardware Key;Carrying Case Keys 2 ; Adapters 3; Battery Charger; USB Cable;Information Manuals and Carrying Case
Medos International Sàrl
91-4205US
Not in Commercial Distribution
- 10886704064947 ()
- 10886704071426 ()
914205US
- Infusion pump programmer
FOR USE WITH: CODMAN 3000 Series Tapered Silicone Rubber Catheter (Radiopaque) with Connector Contents: (1) Catheter: O.D. 2.3mm tapered to O.D. 1.5mm x I.D. 0.6mm x 51.7cm long with (1) Universal Barbed Connector
Medos International Sàrl
IP-37957
In Commercial Distribution
- 10886704044086 ()
IP37957
- Spinal port/catheter
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.
QIAGEN GmbH
V1
In Commercial Distribution
- 04053228034223 ()
873121
- PIK3CA gene mutation IVD, kit, nucleic acid technique (NAT)
QFT-Plus Reference Lab Pack Elisa Kit
QIAGEN SCIENCES INC.
1
In Commercial Distribution
- 04053228015871 ()
622832
- Interferon gamma release IVD, kit, enzyme immunoassay (EIA)
QFT-Plus 2 Plate Elisa Kit
QIAGEN SCIENCES INC.
1
In Commercial Distribution
- 04053228015864 ()
622130
- Interferon gamma release IVD, kit, enzyme immunoassay (EIA)