B. Braun Receives FDA 510(k) Clearance for New DUPLEX System Use

B. Braun has received FDA 510(k) clearance for adding 1 gram and 2 gram Ceflazidime injections within the DUPLEX System, according to a company news release.

The clearance has expanded the number of intravenous therapies the system supports. The 1 and 2 gram Ceflazidime injections can be stored in the DUPLEX System and ready-to-use whenever and wherever it is needed. The DUPLEX System is designed as a two-comparement, flexible, eco-friendly IV container to store pre-measured drug and diluent doses.

Read the release about the new clearance for B. Braun.

More Coverage on B. Braun:

B. Braun Receives Permanent Injunction in Patent Infringement Case

B. Braun Reports 9.8% Sales Growth for FY 2010

B. Braun Announces FDA Approval of OTC Wound Management Gel


Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers