18 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VAPOR-CLEAR, MODEL 100
FDA 510(k)
FDA Class 2
·Anesthesiology
DELTA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252598183·S-DRILLING TAP, HEX, FOR 5/6mm SCREW
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450237748·
MODIFICATION TO THERMAL ANGEL
FDA 510(k)
FDA Class 2
·Hematology
PHACOFRAGMENTATION SYSTEM MEGATRON
FDA 510(k)
FDA Class 2
·Ophthalmic
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 18, 2023
ANGIOJET ULTRA 5000A
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 23, 2019
ANGIOJET ULTRA 5000A
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 23, 2019
ANGIOJET ULTRA 5000A
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 23, 2019
UNKNOWN LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 7, 2017
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·May 3, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 16, 2014
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - TAMPA·Product code FKX·May 18, 2011
MANTIS REDUX BLOCKER
FDA Adverse Event
Malfunction
·STRYKER SPINE-US·Product code NKB·November 27, 2019
TIBIAL NAIL-ADVANCED / 9 345 / STERILE
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·February 27, 2023
TIBIAL NAIL ADVANCED Ø10 L315
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code JDS·April 7, 2023
5.0MM TI LOCKING HEAD SCREW SELF-TAPPING 34MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·June 23, 2023
5.0MM TI LOCKING HEAD SCREW SELF-TAPPING 38MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·June 23, 2023