Ammendment_0001_FDA-15-223-SOL-1151952_Q A.pdf

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Combined Raman, Ultraviolet-Visible Spectrophotometry (UV-VIS) Fluorescence, Spectrometer System
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FDA-15-223-SOL-1151952
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Amendment 0001 FDA-15-223-SOL-1151952 Q A

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FDA-15-223-SOL-1151952_with_Schedule_of_Items.pdf PDF

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Page 1 of 1 FDA-15-223-SOL-1151952

Amendment 0001

The following amendment is to provide the Government’s official response to questions pertaining to Combined Synopsis/Sonication FDA-15-223-SOL-1151952:

Q-1. What are the sample handling requirements (microscopy, macro/cuvette, or both)? If both, please explain in detail.

A-1. Sample handling is through a cuvette.

Q-2. How will the light be delivered to the spectrometer? (fiber-coupled, direct-coupled)

Q-3. What type light source is required for Fluorescence component? Absorbance component?

Q-4. Are all detectors to be configured simultaneously?

A-2 through A-4 Specifics cannot be provided for fiber optic/light source/detector requirements, other than what is already written on the solicitation, since each company may construct the instrument, internal optics, lasers, light sources and detectors differently. Please to refer to the requirements in the solicitation for the combined Raman, Uv-Vis, near IR, Fluorescence spectrometer.

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