23 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NexxZr™ T / D-100-30-NT-D400-SD
FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113856·
Clear Readers
FDA UDI
Diversified Products, Inc.·00037741113232·
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981201012·Interbody, 11mm x 32mm x 17mm, 15 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981208134·Trial, 11mm x 32mm x 17mm, 15 deg
GERBODE NEEDLE HOLDER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896075863·GERBODE NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED...
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981193027·Interbody, 11mm x 32mm x 17mm, 15 deg
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981204860·Trial, 11mm x 32mm x 17mm, 15 Deg
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981190712·Interbody, 11mm x 32mm x 17mm, 15 Deg
RAPIDVUE HCG TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
DESENS-IONOMER
FDA 510(k)
FDA Class 2
·Dental
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·July 25, 2002
OPTISITE ARTERIAL CANNULA
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DQR·June 21, 2024
GENISTRONG
FDA Adverse Event
Malfunction
·GENICON·Product code GCJ·October 15, 2017
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 1, 2014
ACCU-CHEK ® TENDER INFUSION SET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·May 29, 2013
UNKNOWN PRODUCT
FDA Adverse Event
Other
·STRYKER ORTHOPAEDICS CORK·Product code MRA·June 6, 2011
OPTISITE ARTERIAL CANNULA
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DQR·June 21, 2024
SWARTZ¿ INTRODUCER, UNKNOWN
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code DYB·March 25, 2020
AGILIS¿ INTRODUCER, UNKNOWN
FDA Adverse Event
Death
·ST. JUDE MEDICAL, COSTA RICA LTDA·Product code DYB·March 25, 2020