9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
PURITAN-BENNETT OXYGEN PRESSURE REGULATOR
FDA 510(k)
FDA Class 1
·Anesthesiology
Novo Surgical Inc.
FDA UDI
NOVO SURGICAL, INC.·00842331134425·mcglamry metatarsal elevator, sharp, 6 1/2" (16...
LEONE SPA
FDA UDI
LEONE SPA·08033707085058·WEB I MOL BANDS G8424-16+G2820-00 LR 28
PATIENT EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
FACELOCK FILTER MASK
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 10, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 22, 2014
CRE(TM) BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KOG·November 10, 2010
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 12, 2020