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Construction & real estate›💡Electronic & Electrical›🍎Food & Beverages›🛋️Home furnishing & supplies›⚗️Industrial goods & chemical›🪨Minerals & metals›📦Miscellaneous›











Mexico hosts Aconitum Comercializadora, which currently lists twelve active products across medical, diagnostic and industrial categories. The catalogue includes Swab Kits VTM UTM PCR (HS 3821.00) with synthetic flocked tips, PCR Automatic Machine, Covid Rapid Antibody Test Kits (HS 3822.00), Alcohol Ethyl 70 % (HS 2207.20), Alcohol Isopropyl (HS 2905.12), Disinfectant Wipes, Spray Alcohol Disinfectant, N95 Face Masks, Military/Police Leather Boots, Dead Body Plastic Bags PostMortem, and Access Bio Care Start Covid‑19 Antigen Test Kit (HS 3822.00). The listed HS codes fall within Chapter 38 (pharmaceutical preparations), Chapter 22 (beverages and alcohol), Chapter 29 (organic chemicals) and Chapter 30 (pharmaceutical products). Each product description includes the principal material, such as nitrocellulose membranes for rapid test kits or polypropylene/HDPE tubes for swab kits. The supplier’s active product count of twelve reflects a diversified portfolio that spans personal protective equipment, diagnostic reagents and industrial chemicals.
From the catalogue, Aconitum Comercializadora provides swab kits with synthetic flocked tips, a viral transport medium housed in PP/HDPE tubes, and rapid immunochromatographic test kits that use nitrocellulose membranes and colloidal gold conjugates. In the medical PPE segment the N95 masks correspond to filtration efficiency of at least 95 % for 0.3 µm particles, complying with US NIOSH 42CFR Part 84 or EN 149 standards. The ethanol and isopropyl alcohol are supplied at typical commercial concentrations of 70 % and 99 % respectively, meeting WHO disinfection formulations and requiring material safety data sheets (SDS). Plastic dead‑body bags are usually manufactured from 30‑60 µm polypropylene, offering puncture resistance and a capacity of 30‑40 L per bag. Diagnostic kits generally aim for sensitivity above 90 % and specificity above 95 %, and are often CE‑marked under the IVD directive or hold FDA Emergency Use Authorization.
Swab Kits VTM UTM PCR are classified under HS 3821.00 (pharmaceutical preparations), while Covid Rapid Antibody Test Kits and Access Bio Care Start Covid‑19 Antigen Test Kit fall under HS 3822.00 (diagnostic preparations). The Test Kits Rapid COVID‑19 Healgen are listed under HS 3002.15 (pharmaceutical preparations of other kind).
Buyers should request NIOSH 42CFR Part 84 certification for US compliance, EN 149 certification for European markets, and any applicable CE marking that confirms conformity with personal protective equipment directives.
Standard documentation includes a material safety data sheet (SDS), a certificate of analysis (COA) showing concentration and purity, and compliance statements for GHS labeling. For shipments to the EU, REACH registration may also be required.
The bags are typically made from 30‑60 µm polypropylene, have a capacity of 30‑40 L, and are packed in bulk cartons containing 200 bags each. Each carton is sealed and labeled according to hazardous waste transport regulations when required.
Lead times for a fully assembled PCR Automatic Machine usually range from eight to twelve weeks after order confirmation, depending on component availability and customization requirements.
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