32 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIQUICHEK IMMUNOLOGY CONTROL, LEVEL 1,2,3, TRILEVEL MINIPAK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925033382·BUCK WAX CURETTE DISPOSABLE SIZE 2 (6/PK)
DELTA XTEND
FDA UDI
DEPUY (IRELAND)·10603295502609·DELTA XTEND Lateralized Glenosphere +0mm Eccent...
DELTA XTEND
FDA UDI
DEPUY (IRELAND)·10603295502562·DELTA XTEND Lateralized Glenosphere +0mm Standa...
DELTA XTEND
FDA UDI
DEPUY (IRELAND)·10603295502593·DELTA XTEND Lateralized Glenosphere +0mm Eccent...
DELTA XTEND
FDA UDI
DEPUY (IRELAND)·10603295502555·DELTA XTEND Lateralized Glenosphere +0mm Standa...
KAISHOU VAGINAL SPECULUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BIOPRO POLAR HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
GUIDE WIRE, SMOOTH-TIPPED, STERILE T2 HUMERUS Ø2,2X800 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·December 2, 2015
GUIDE WIRE, BALL-TIPPED, STERILE T2 HUMERUS Ø2.5X800 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·December 2, 2015
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024494893·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024494909·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024494916·
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 24, 2013
QUADRA ASSURA MP CRT-D, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·September 30, 2014
REVO MRI SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWP·June 16, 2011
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 26, 2024
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·October 6, 2022
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 15, 2020
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·February 9, 2023