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World Leading Filtration, Breathability, and Fit. The CAN99™ 9500 Surgical Respirator was Designed to Provide the Highest Level of Protection of Any Disposable Respirator. · NIOSH Certified N95 Surgical Respirator (PT-C99-9500-01M) · CE FFP3 Certified (EN149) · Health Canada Authorized · CSA Certified (99PFE-L3) >99% Filtration (FFP3) >95% Filtration (NIOSH) Industry-Leading Breathability ASTM Level 3 Surgical Respirator (>160 mmHg blood penetration resistance) Passes Quantitative Fit Testing Across 88-92% of Face sizes Headband Donning for a Proper Tight Seal Fully Aluminum Nose Piece (MRI compatible) Graphene-Free
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Our product line is led by our ultra-long acting, low-toxicity local anesthetic medication, Enduracaine™. Enduracaine™ is a novel combination of three well-known, extremely safe and effective local anesthetics. The combination delivers advanced pain management performance, something that the much-hyped liposomal encapsulated bupivacaine never delivered. Enduracaine™ produces an aqueous solution of 0.4% lidocaine with 0.2% tetracaine and 4mcg per milliliter of epinephrine. Ventis Pharma is in the FDA fast-track approval process for this product. We plan to introduce an intermediate, off-label kit version of the drug compound as we await approval for the ultimate, extremely user-friendly version of Enduracaine™. We also plan to introduce a low-dose oral analgesic formulation as part of our work in developing pain management solutions. Ventis Pharma is conducting ongoing research into user-friendly, moderate-cost adjuvants to enhance other local anesthetic applications. Given recent consensus statements from the American Society of Anesthesiologists in their publication “Anesthesiology” regarding the lack of efficacy of the liposomal encapsulated bupivacaine products, we believe there is a growing need for safe and effective local anesthetic products and adjuvants. While there are other drugs in the FDA approval process that claim to provide an extended local anesthetic effect, they all utilize some formulation of the local anesthetic bupivacaine, which has a long history of significant cardiovascular risks. Worryingly, there are also formulations in the approval process which combine this toxic drug with a non-steroidal anti-inflammatory drug that was removed from the market due to adverse drug reaction concerns.
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The Rapid SARS-CoV-2 Antigen Test Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2. This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older, or with adult-collected anterior nasal (nares) swab samples from individuals aged 2 years or older when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests. The test is authorized for individuals aged 2 years and older with symptoms of COVID-19 within the first 6 days of symptom onset, or individuals without symptoms or other epidemiological reasons to suspect COVID-19.
