fda
2 records
FDA Recall: B. Braun Interventional Systems — Class II
20150819
The manufacturer, B. Braun medical France, received endotoxin test results that are out of specification for the peelable sheath (A1537). | Product: Celsite Implantable Access Port System, model ST301...
View Source
FDA Device Recall: Celsite Implantable Access Port System, model ST301. The Celsite Implantable Ac
2015-08-19
Class II — The manufacturer, B. Braun medical France, received endotoxin test results that are out of specification for the peelable sheath (A1537).
View Source
ny_corps
1 records
NY Corp: B. BRAUN INTERVENTIONAL SYSTEMS INC.
2006-11-16
FOREIGN BUSINESS CORPORATION | County: Nassau | Jurisdiction: Delaware
View Source
Be informed when major changes happen on C.F.A.I. — new data sources, platform updates, critical enforcement alerts
No spam. Only major updates. Unsubscribe anytime.