Attachments V - Brand Name or Equal Compliance Matrix .xlsx

This file is a Brand Name or Equal Compliance Matrix for a semiautomatic aerosol propellant filler procurement by the FDA's Center for Drug Evaluation and Research. The matrix outlines mandatory equipment specifications and compliance requirements that offerors must address in their quotations, including a pressure filler with column and base plate, stainless steel pneumatic control box, adjustable dosing cylinder (0.5-20 ml), diaphragm shut-off valve, and AISI 316L product-contact components. The equipment must support oil-free operation, quick-change product aggregate, quick-release couplings, 2002/100 crimper functionality, and 20 mm valve capability with adjustable crimp height and diameter.

Additional mandatory specifications include two-hand safety release mechanism, crimp height measuring gauge, digital display gauge, propellant pump capacity up to 15 L/min, maximum outlet pressure of 2,000 kPa, and compatibility with LPG, DME, and HFA propellants. Offerors must also provide Factory Acceptance Test documentation, validation documentation with support, installation services, training, a one-year warranty with onsite repairs, and delivery within 90 calendar days. Quotations must be submitted electronically to Michele.Jackson@fda.hhs.gov no later than June 22, 2026, at 11:00 AM Eastern Time, with the subject line including the company name and solicitation number 75F40126Q00231/CDER-2026-133243. Written questions regarding the requirement must be submitted by June 15, 2026, at 9:00 AM Eastern Time.