BD Receives CE Mark for Revello™ Vascular Covered Stent
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1 hour ago
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Should l Buy BDX?
Source: PRnewswire
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE marking, a significant advancement aimed at treating peripheral artery disease in the aging EU population, which is expected to enhance the company's competitive position in the European market.
- Technological Innovation: The Revello™ stent combines the flexibility of a self-expanding Nitinol stent with radial resistance tailored for iliac arteries, designed to improve treatment outcomes and reduce complication risks, thereby enhancing physicians' capabilities in complex cases.
- Clinical Research Support: The clinical performance of the stent is being evaluated in the AGILITY multicenter study led by the Chair of Vascular Surgery at Cleveland Clinic, which is expected to provide robust data to support its market launch and further solidify BD's leadership in peripheral vascular treatments.
- Market Launch Strategy: The Revello™ stent will be introduced in countries accepting the CE mark, anticipated to generate new revenue streams for BD while increasing its influence in the global medical device market, particularly in the rapidly growing European sector.
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Analyst Views on BDX
Wall Street analysts forecast BDX stock price to rise
11 Analyst Rating
5 Buy
6 Hold
0 Sell
Moderate Buy
Current: 171.490
Low
157.00
Averages
192.64
High
232.00
Current: 171.490
Low
157.00
Averages
192.64
High
232.00
About BDX
Becton, Dickinson and Company is a global medical technology company. The Company is engaged in the development, manufacture and sale of a broad range of medical supplies, devices, laboratory equipment and diagnostic products used by healthcare institutions, physicians, life science researchers, clinical laboratories, and more. It operates through four segments: BD Medical Essentials, BD Connected Care, BD BioPharma Systems and BD Interventional. BD Medical Essentials segment includes medication delivery solutions and specimen management. BD Connected Care segment includes medication management solutions and advanced patient monitoring. BD Interventional segment includes urology and critical care, peripheral intervention and surgery.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
BD Receives CE Mark for Revello™ Vascular Covered Stent
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE marking, a significant advancement aimed at treating peripheral artery disease in the aging EU population, which is expected to enhance the company's competitive position in the European market.
- Technological Innovation: The Revello™ stent combines the flexibility of a self-expanding Nitinol stent with radial resistance tailored for iliac arteries, designed to improve treatment outcomes and reduce complication risks, thereby enhancing physicians' capabilities in complex cases.
- Clinical Research Support: The clinical performance of the stent is being evaluated in the AGILITY multicenter study led by the Chair of Vascular Surgery at Cleveland Clinic, which is expected to provide robust data to support its market launch and further solidify BD's leadership in peripheral vascular treatments.
- Market Launch Strategy: The Revello™ stent will be introduced in countries accepting the CE mark, anticipated to generate new revenue streams for BD while increasing its influence in the global medical device market, particularly in the rapidly growing European sector.
See More
BD Launches New Revello™ Vascular Stent
- CE Mark Approval: BD announced that its Revello™ vascular stent has received CE marking, marking a significant advancement in treating lower limb arterial diseases, which is expected to greatly enhance physicians' capabilities in managing complex cases and meet the growing market demand.
- Technological Innovation: The Revello™ stent combines a self-expanding nitinol structure with radial resistance suitable for iliac arteries, designed to improve vessel patency while reducing the risk of trauma to healthy vascular segments, thereby enhancing patient treatment outcomes and safety.
- Clinical Trial Support: The ongoing AGILITY clinical trial, led by experts from the Cleveland Clinic, aims to evaluate the stent's performance in patients with peripheral artery disease, further validating its clinical application effectiveness.
- Market Launch Plan: The Revello™ stent will be launched in European countries accepting CE marking, which is expected to strengthen BD's competitiveness in the European market, while it remains experimental in the U.S., limiting its usage scope.
See More
BD Receives CE Mark for Revello Vascular Stent
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE Marking, representing a significant advancement in the treatment of atherosclerotic lesions in the iliac arteries, crucial for addressing complex peripheral artery disease.
- Clinical Trial Support: The ongoing AGILITY clinical trial, led by Dr. Sean Lyden from Cleveland Clinic, evaluates the device's performance in patients with peripheral artery disease, further validating its clinical efficacy and potential impact on treatment protocols.
- Technical Advantages: The stent combines the flexibility of a self-expanding stent with radial resistive force tailored for iliac arteries, featuring an ultrathin expanded polytetrafluoroethylene covering designed to maintain artery patency while minimizing trauma to healthy vessel segments, enhancing treatment safety and effectiveness.
- Broad Market Prospects: The Revello™ Stent will be launched in CE-mark-accepting countries across Europe, expected to strengthen BD's competitive position in the peripheral vascular market while providing physicians with more precise treatment options to meet the growing healthcare demands.
See More
BD Receives CE Mark for Revello Vascular Stent
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE Marking, representing a significant advancement in treating atherosclerotic lesions in the iliac arteries, crucial for addressing complex peripheral artery disease.
- Technological Innovation: The Revello™ Stent combines the flexibility of a self-expanding stent with radial resistive force tailored for iliac arteries, featuring an ultrathin expanded polytetrafluoroethylene covering designed to keep arteries open while minimizing trauma to healthy vessel segments.
- Clinical Trial Support: The stent was introduced at the LINC 2026 congress in Germany, where physicians discussed its potential impact on iliac interventions, and the ongoing AGILITY clinical trial will evaluate its performance in patients with peripheral artery disease.
- Market Launch Plan: The Revello™ Stent will be launched in CE-mark-accepting countries across Europe, further expanding BD's peripheral vascular portfolio and enhancing the company's competitive position in the medical technology market.
See More
BD Launches First Antimicrobial Irrigation System with FDA Clearance
- FDA Clearance: BD's Surgiphor™ 1000mL has received 510(k) clearance from the FDA, making it the first 1000 mL antimicrobial irrigation system specifically designed for powered lavage, reinforcing the company's leadership in surgical irrigation innovation.
- Enhanced Surgical Efficiency: This system simplifies complex surgical procedures by providing a standardized, ready-to-use antimicrobial solution, enabling surgical teams to efficiently remove debris and microorganisms from wounds, thereby improving patient care quality.
- Compatibility and Flexibility: Surgiphor™ 1000mL is compatible with many commonly used powered irrigation devices and includes an adapter and Y-connector for quick switching between saline and Surgiphor™ solution, enhancing operational flexibility in the operating room.
- Global Safety Standards: The launch of this product not only saves valuable time in the operating room but also helps hospitals meet global safety guidelines for surgical wound cleaning, further solidifying BD's market position in the medical technology sector.
See More
BD Launches First Antimicrobial Irrigation System
- FDA Clearance: BD's Surgiphor™ 1000mL has received 510(k) clearance from the U.S. FDA, becoming the first and only 1000mL antimicrobial irrigation system designed for powered lavage, reinforcing the company's leadership in surgical irrigation innovation.
- Enhanced Surgical Efficiency: This system provides a standardized, ready-to-use solution that simplifies the wound cleaning process during complex surgeries, enabling surgical teams to efficiently remove debris and microorganisms, thereby improving surgical safety and efficacy.
- Time Savings in OR: The Surgiphor™ 1000mL arrives fully sterile and ready to use, eliminating the need for hospital staff to mix solutions manually, which saves valuable time in the operating room and helps hospitals meet global safety standards for surgical wound cleaning.
- Flexible Irrigation Configurations: The new product expands the Surgiphor™ portfolio by offering both manual and powered irrigation configurations, allowing clinicians to choose based on workflow and patient needs, further enhancing adaptability in surgical procedures.
See More
BD Receives CE Mark for Revello™ Vascular Covered Stent
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE marking, a significant advancement aimed at treating peripheral artery disease in the aging EU population, which is expected to enhance the company's competitive position in the European market.
- Technological Innovation: The Revello™ stent combines the flexibility of a self-expanding Nitinol stent with radial resistance tailored for iliac arteries, designed to improve treatment outcomes and reduce complication risks, thereby enhancing physicians' capabilities in complex cases.
- Clinical Research Support: The clinical performance of the stent is being evaluated in the AGILITY multicenter study led by the Chair of Vascular Surgery at Cleveland Clinic, which is expected to provide robust data to support its market launch and further solidify BD's leadership in peripheral vascular treatments.
- Market Launch Strategy: The Revello™ stent will be introduced in countries accepting the CE mark, anticipated to generate new revenue streams for BD while increasing its influence in the global medical device market, particularly in the rapidly growing European sector.
See More
BD Launches New Revello™ Vascular Stent
- CE Mark Approval: BD announced that its Revello™ vascular stent has received CE marking, marking a significant advancement in treating lower limb arterial diseases, which is expected to greatly enhance physicians' capabilities in managing complex cases and meet the growing market demand.
- Technological Innovation: The Revello™ stent combines a self-expanding nitinol structure with radial resistance suitable for iliac arteries, designed to improve vessel patency while reducing the risk of trauma to healthy vascular segments, thereby enhancing patient treatment outcomes and safety.
- Clinical Trial Support: The ongoing AGILITY clinical trial, led by experts from the Cleveland Clinic, aims to evaluate the stent's performance in patients with peripheral artery disease, further validating its clinical application effectiveness.
- Market Launch Plan: The Revello™ stent will be launched in European countries accepting CE marking, which is expected to strengthen BD's competitiveness in the European market, while it remains experimental in the U.S., limiting its usage scope.
See More
BD Receives CE Mark for Revello Vascular Stent
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE Marking, representing a significant advancement in the treatment of atherosclerotic lesions in the iliac arteries, crucial for addressing complex peripheral artery disease.
- Clinical Trial Support: The ongoing AGILITY clinical trial, led by Dr. Sean Lyden from Cleveland Clinic, evaluates the device's performance in patients with peripheral artery disease, further validating its clinical efficacy and potential impact on treatment protocols.
- Technical Advantages: The stent combines the flexibility of a self-expanding stent with radial resistive force tailored for iliac arteries, featuring an ultrathin expanded polytetrafluoroethylene covering designed to maintain artery patency while minimizing trauma to healthy vessel segments, enhancing treatment safety and effectiveness.
- Broad Market Prospects: The Revello™ Stent will be launched in CE-mark-accepting countries across Europe, expected to strengthen BD's competitive position in the peripheral vascular market while providing physicians with more precise treatment options to meet the growing healthcare demands.
See More
BD Receives CE Mark for Revello Vascular Stent
- CE Mark Achievement: BD announced that its Revello™ Vascular Covered Stent has received CE Marking, representing a significant advancement in treating atherosclerotic lesions in the iliac arteries, crucial for addressing complex peripheral artery disease.
- Technological Innovation: The Revello™ Stent combines the flexibility of a self-expanding stent with radial resistive force tailored for iliac arteries, featuring an ultrathin expanded polytetrafluoroethylene covering designed to keep arteries open while minimizing trauma to healthy vessel segments.
- Clinical Trial Support: The stent was introduced at the LINC 2026 congress in Germany, where physicians discussed its potential impact on iliac interventions, and the ongoing AGILITY clinical trial will evaluate its performance in patients with peripheral artery disease.
- Market Launch Plan: The Revello™ Stent will be launched in CE-mark-accepting countries across Europe, further expanding BD's peripheral vascular portfolio and enhancing the company's competitive position in the medical technology market.
See More
BD Launches First Antimicrobial Irrigation System with FDA Clearance
- FDA Clearance: BD's Surgiphor™ 1000mL has received 510(k) clearance from the FDA, making it the first 1000 mL antimicrobial irrigation system specifically designed for powered lavage, reinforcing the company's leadership in surgical irrigation innovation.
- Enhanced Surgical Efficiency: This system simplifies complex surgical procedures by providing a standardized, ready-to-use antimicrobial solution, enabling surgical teams to efficiently remove debris and microorganisms from wounds, thereby improving patient care quality.
- Compatibility and Flexibility: Surgiphor™ 1000mL is compatible with many commonly used powered irrigation devices and includes an adapter and Y-connector for quick switching between saline and Surgiphor™ solution, enhancing operational flexibility in the operating room.
- Global Safety Standards: The launch of this product not only saves valuable time in the operating room but also helps hospitals meet global safety guidelines for surgical wound cleaning, further solidifying BD's market position in the medical technology sector.
See More
BD Launches First Antimicrobial Irrigation System
- FDA Clearance: BD's Surgiphor™ 1000mL has received 510(k) clearance from the U.S. FDA, becoming the first and only 1000mL antimicrobial irrigation system designed for powered lavage, reinforcing the company's leadership in surgical irrigation innovation.
- Enhanced Surgical Efficiency: This system provides a standardized, ready-to-use solution that simplifies the wound cleaning process during complex surgeries, enabling surgical teams to efficiently remove debris and microorganisms, thereby improving surgical safety and efficacy.
- Time Savings in OR: The Surgiphor™ 1000mL arrives fully sterile and ready to use, eliminating the need for hospital staff to mix solutions manually, which saves valuable time in the operating room and helps hospitals meet global safety standards for surgical wound cleaning.
- Flexible Irrigation Configurations: The new product expands the Surgiphor™ portfolio by offering both manual and powered irrigation configurations, allowing clinicians to choose based on workflow and patient needs, further enhancing adaptability in surgical procedures.
See More
