9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
FORCEPS, BIOPSY, GASTROINTESTINAL
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
SeaSpine Spacer System - Hollywood™
FDA UDI
Seaspine Orthopedics Corporation·10889981058401·16mm Hollywood Trial, Lordotic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471183797·K-WIRE - SINGLE TROCAR 1.8mm DIA x 150mm
SeaSpine Spacer System - Hollywood™
FDA UDI
Seaspine Orthopedics Corporation·10889910058403·16mm Hollywood Trial, Lordotic
SITE DIAPHRAGM CASSETTE
FDA 510(k)
FDA Class 1
·Ophthalmic
JAKOBI SURG. INSTRUMENTS #11
FDA 510(k)RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·December 8, 2010
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014