13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LARYNGOSCOPE RIGID
FDA 510(k)
FDA Class 1
·Anesthesiology
36M - Class B 21 - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620190·36M - Class B 21 - Metal
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150607·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 230mm
SunTech Tango M2 Kit
FDA UDI
MORTARA INSTRUMENT, INC.·00812345029765·SUNTECH TANGO M2 BP MONITOR KIT QS/X V6
STREPTOCOCCUS APP. SEROLOGICAL REAGENTS
FDA 510(k)
FDA Class 1
·Microbiology
PERIFIX CATHETER CONNECTOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ZMR®
FDA UDI
Zimmer, Inc.·00889024157125·
ZMR®
FDA UDI
Zimmer, Inc.·00889024157118·
ZMR®
FDA UDI
Zimmer, Inc.·00889024157101·
EPIC SUPRA STENTED TISSUE VALVE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA)·Product code LWR·December 12, 2019
AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - ANTERIOR
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code OTP·January 4, 2013
NEW LIGASURE 5MM
FDA Adverse Event
Malfunction
·COVIDIEN LP (VALLEYLAB)·Product code GEI·December 8, 2010
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·July 9, 2014