BioCardia Receives CE Mark Renewal For Helix Biotherapeutic Delivery Catheter And Morph Guide Catheter Through May 2024
BioCardia, Inc. (BCDA)
US:NASDAQ Investor Relations:
biocardia.com/investors/press-releases/id/1037?pressreleaseid=41
Company Research
Source: GlobeNewswire
SAN CARLOS, Calif., Oct. 08, 2019 (GLOBE NEWSWIRE) -- BioCardia (Nasdaq: BCDA), a leader in the development of comprehensive solutions for cardiovascular regenerative therapies, today announced renewal of the CE Mark for the Helix™ Biotherapeutic Delivery Catheter and Morph® Universal Deflectable Guide Catheter, both used in the delivery of biotherapeutics to the heart. CE Mark renewal enables BioCardia to continue supporting partners conducting biotherapeutic clinical trials outside of the U.S., such as CellProThera and Centro Cardiologico Monzino, as well as commercial sales in the European Union and other countries that recognize the CE Mark through May 2024. “Renewal of the CE Mark for our innovative biotherapeutic delivery products ensures that we can continue participating in a variety of biotherapeutic research programs with the potential to drive the field forward and respond to very ill patients,” said BioCardia CEO Peter Altman. “In light of sweeping European regulat
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BCDA
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- 11/8/23 - In-Line
BCDA
Sec Filings
- 4/19/24 - Form 4
- 4/15/24 - Form DEF
- 4/5/24 - Form SC
- BCDA's page on the SEC website