SEARCH RESULTS FOR: 购买假的单位存款证明【咨询网:ｚｊｗ２１１.ｃｏｍ】宜城得克萨斯A(2872641 results)
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content:
- carrying bag A/N100503
- USB Cable A/N100418
- AuDX PRO Flex A/N100434-AUPF
- Probe EP-TY A/N100188-US
- Insert Earphone Bio- Logic A/N100860-BL
- Bone Conductor B71 A/N100344
- Gooseneck Microphone A/N100779
- FW Reflex & Tymp Class1 A/N100561
- FW TEOAE A/N100109
- FW DPOAE A/N100110
- FW FMDPOAE A/N100536
- FW DPHiRES A/N100537
- FW Mira PC- Software A/N100116
- FW PTA3 A/N100114
- FW High Frequency A/N100454
- FW Magic A/N100112
- FW Labelprinter A/N100414
- Accessory Box Combo A/N100261
- Power Supply Senti/Sentiero Desktop US A/N100524
- User Manual A/N100904-EN-BL
- Test Cavity Tymp A/N100549
PATH medical GmbH
100497-BLP1
Not in Commercial Distribution
- 04260223143359 ()
- Evoked-potential audiometer
No Description
THE BINDING SITE GROUP LIMITED
NK626.T.A
In Commercial Distribution
- 05051700017008 ()
- Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry
No Description
THE BINDING SITE GROUP LIMITED
NK625.T.A
In Commercial Distribution
- 05051700016995 ()
- Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry
ViraDx™ SARS-CoV-2/Flu A+B Rapid Antigen Test Kit, 25 tests
Lumos Diagnostics, Inc.
CP0031
In Commercial Distribution
- 00850056728706 ()
CP0031
- SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical
- Influenza A/B virus antigen IVD, kit, rapid ICT, clinical
The Nano-Check™ Influenza+COVID-19 Dual Test is a lateral flow immunochromatographic assay intended for in vitro rapid, simultaneous qualitative detection and differentiation of influenza A, and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid antigen directly from anterior nasal swab specimens of individuals with signs and symptoms of respiratory infection consistent with COVID-19 within the first five (5) days of symptom onset when tested at least twice over three days with at least 48 hours between tests. Clinical signs and symptoms of respiratory viral infection due to SARS-CoV-2 and influenza can be similar. The Nano-Check™ Influenza+COVID-19 Dual Test is only for in vitro diagnostic use under the Food and Drug Administration’s Emergency Use Authorization. This product has not been cleared or approved.
NANO-DITECH CORPORATION
MD8151E
In Commercial Distribution
- 10895160002844 ()
- 00895160002847 ()
- Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, clinical
The Alethia™ Group A Streptococcus (Group A Strep) assay, performed on the Alethia™ Instrument, is a qualitative in vitro diagnostic test for the detection of Streptococcus pyogenes (Group A beta-hemolytic Streptococcus) in throat swab specimens. The Alethia™ Group A Strep assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Streptococcus pyogenes by targeting a segment of the Streptococcus pyogenes genome. Results from the Alethia™ Group A Strep assay can be used as an aid in the diagnosis of Group A Streptococcal pharyngitis. The assay is not intended to monitor treatment for Group A Streptococcus infections.
MERIDIAN BIOSCIENCE, INC.
480150
In Commercial Distribution
- 00840733102264 ()
480150
- Beta-haemolytic Group A Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)
The Alethia™ Group A Streptococcus (Group A Strep) External Control Kit contains Positive Reagent for use with the Alethia™ Group A Streptococcus DNA Amplification Assay. The External Positive Control Reagent is used in conjunction with the Alethia™ Sample Preparation Apparatus II/Negative Control III reagent provided with the Group A Strep Kit as part of routine Quality Control Testing. External controls are used as part of a routine quality control program.
MERIDIAN BIOSCIENCE, INC.
479910
In Commercial Distribution
- 00840733102127 ()
479910
- Streptococcus mutans group antigen IVD, calibrator
The illumigene Group A Streptococcus (Group A Strep) assay, performed on the illumipro-10, is a qualitative in vitro diagnostic test for the detection of Streptococcus pyogenes (Group A beta-hemolytic Streptococcus) in throat swab specimens.
The illumigene Group A Strep assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Streptococcus pyogenes by targeting a segment of the Streptococcus pyogenes genome. Results from the illumigene Group A Strep assay can be used as an aid in the diagnosis of Group A Streptococcal pharyngitis. The assay is not intended to monitor treatment for Group A Streptococcus infections.
MERIDIAN BIOSCIENCE, INC.
280150
Not in Commercial Distribution
- 00840733101335 ()
280150
- Beta-haemolytic Group A Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)
Status™ COVID-19/Flu A&B Antigen test kit, 25 tests
PRINCETON BIOMEDITECH CORPORATION
BSP-511-25
In Commercial Distribution
- 10743816001553 ()
BSP-511-25
- SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical
- Influenza A/B virus antigen IVD, kit, rapid ICT, clinical
T & A
MEDLINE INDUSTRIES, INC.
DYNJ901895
In Commercial Distribution
- 10888277848900 ()
DYNJ901895
- General surgical procedure kit, non-medicated, reusable