21 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARTHREX WRIST BIO-ANCHOR, MODEL AR-1322B
FDA 510(k)
FDA Class 2
·Orthopedic
Safco Peeso Reamers
FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310222343·Safco peeso reamers, #01, 32mm, 6/box
Logical Dual Mobility Poly Insert
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215112424·
VKS KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
A1CNOW FOR RX HOME USE
FDA 510(k)
FDA Class 2
·Hematology
3.0MM HEX DRIVER
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·March 7, 2024
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022234855231317201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222348552338117201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222348552315917201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022234855231217201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222348552312717201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022234855232517201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222348552338217201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0222348552312017201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022234855233217201·RITE-TRT
WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NGV·February 8, 2022
COULTER® ACT DIFF 12¿ ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·March 26, 2013
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD.·Product code JAA·February 28, 2011
SILICONE ADVANCED OPTIC-VIOLET SHIELD
FDA Adverse Event
Malfunction
·BAUSCH & LOMB·Product code HQL·March 26, 2008
AIA-2000
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·October 4, 2019