188 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COSMAN RF LESION GENERATOR, MODEL RFG-1A; COSMAN TEW TRIGEMINAL ELECTRODE KIT; COSMAN TIC TRIGEMINAL ELECTRODE KIT;
FDA 510(k)
FDA Class 2
·Neurology
TruLock
FDA UDI
Rmo, Inc.·00885797648013·TRULOCK Primer Activated Adhesive Mini Kit (1ea...
MedGyn Pessary Marland w/ support # 2
FDA UDI
MEDGYN PRODUCTS, INC.·M803050084·Marland Pessary is used to treat uterine prola...
Copper Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989025705·PREF.LING.ARCH 35 CUNITI 017X025 UP SZ3 PK10
basixCOMPAK™
FDA UDI
Merit Medical Systems, Inc.·00884450024362·
Disposable Cuff
FDA UDI
SUNTECH MEDICAL, INC.·10840935109310·
NA
FDA UDI
STRYKER CORPORATION·07613327051629·Fiber Optic Light Cable, Opaque
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·August 10, 2017
REAL PATIENT REAL PATIENT 128 CHANNEL EEG HEADBOX, MODEL EX-NW-128-RP
FDA 510(k)
FDA Class 2
·Neurology
ENRAF-NONIUS SONOPULS 190 SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
CENTERPIECE? PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code NQW·April 16, 2015
CENTERPIECE¿ PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·June 8, 2016
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·April 10, 2013
BIPOLAR LEAD MODEL 300
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·March 31, 2011
ACUVUE OASYS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON·Product code LPL·May 21, 2008
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·December 7, 2017
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019