28 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ETHIBOND EXCEL VALVE LOOP SUTURE
FDA 510(k)
FDA Class 2
·Cardiovascular
Oph. Cystotomes
FDA UDI
KATENA PRODUCTS, INC.·00841668113714·CYSTOTOME REVERSED FORM 25GA
CorticaLINK
FDA UDI
LINKSPINE, INC.·00817329020158·5.0mm Titanium Rod: 70mm Straight
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·04546540503831·POSTERIOR PLANE PROBE
FLOCATH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RADIOMED SOURCE
FDA 510(k)
FDA Class 2
·Radiology
MultiPolar®
FDA UDI
Zimmer, Inc.·00889024116320·
MultiPolar®
FDA UDI
Zimmer, Inc.·00889024116344·
MultiPolar®
FDA UDI
Zimmer, Inc.·00889024116337·
C-SHAPE SLV RDCTN STYLE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE·Product code NKB·December 13, 2016
C-SHAPE SLV RDCTN STYLE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE·Product code NKB·December 13, 2016
OPEN IMPLANT CLOSURE TOP
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE·Product code NKB·December 13, 2016
C-SHAPE SLV RDCTN STYLE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE·Product code NKB·December 13, 2016
OPEN IMPLANT CLOSURE TOP
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE·Product code NKB·December 13, 2016
OPEN IMPLANT CLOSURE TOP
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE·Product code NKB·December 13, 2016
APTIMA SARS-COV-2/FLU MULTIPLEX ASSAY
FDA Adverse Event
Malfunction
·HOLOGIC INCORPORATED·Product code QLT·December 24, 2021
APTIMA SARS-COV-2/FLU MULTIPLEX ASSAY
FDA Adverse Event
Malfunction
·HOLOGIC INCORPORATED·Product code QLT·December 24, 2021
QIAcube Connect MDx, Model No. 9003070
FDA Recall
Open, Classified
·Qiagen Sciences LLC·Product code JJH·November 21, 2021
SOLYX SIS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·March 13, 2013
TROCHANTERIC NAIL KIT, TI 11X180MM X 125
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·February 8, 2011