Web13 de abr. de 2024 · 암젠(Amgen)의 연도별 주요 연혁 Amgen Inc.는 1980년에 설립된 미국의 생명공학 회사이며 1980년에 설립되었고 1983년에 처음으로 인터페론 베타를 생산및 허가 바았으며, 1987년에 에리스로포이어틴(Erythropoietin)을 생산 및허가 받았으며, 1991년에 열성호중구감소증에 대한 화학요법 치료제인 Neupogen을 생산 ... WebResolute Onyx drug-eluting stent (DES) offers flexibility, 1 conformability, 1 a 2.0-5.0 mm size matrix, and is indicated for high bleeding risk patients and labeled for one-month DAPT. 2 Product specifications Resolute Onyx DES — rapid exchange coronary stent system Rapid exchange ordering details (opens new window)
Medtronic receives FDA approval for latest generation drug …
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Medtronic’s Resolute Onyx DES secures FDA approval
WebApollo Onyx Delivery Microcatheter: Generic Name: Agent, Injectable, Embolic: Applicant: EV3 NEUROVASCULAR: Date Received: 2024-08-21: Decision Date: 2024-12-10: PMA: … WebBIOTRONIK announced today it received U.S. Food and Drug Administration (FDA) approval of its Orsiro® Mission bioabsorbable polymer coronary drug-eluting stent system (BP-DES). The company also announced the first US implant and full commercial availability in … Web1 de jul. de 2024 · Medtronic announced the FDA had granted approval to the Onyx Frontier drug-eluting stent (DES) for treatment of patients with coronary artery disease in a press release on May 13. In their release, Medtronic noted the Onyx Frontier will be available in 2.0 mm sizes as well as 4.50-5.00 mm sizes that can be expanded to 6.00 mm. nsha executive team