11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IOB DISPOSABLE SPECULUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AXOGUARD NERVE CONNECTOR AND PROTECTOR
FDA Adverse Event
Injury
·COOK BIOTECH·Product code JXI·August 24, 2015
ETEST TOBRAMYCIN 0.016-256 UG/ML AND 0.064-1024 UG/ML
FDA 510(k)
FDA Class 2
·Microbiology
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 7, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·October 1, 2014
PRODISC-L INSERTER F/SIZE M
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·May 29, 2013
ROCHE OMNI 1
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CHL·June 17, 2011
AXOGUARD NERVE CONNECTOR AND PROTECTOR
FDA Adverse Event
Injury
·COOK BIOTECH·Product code JXI·October 24, 2019
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 20, 2012
SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·May 16, 2017