22 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Digital Automatic Blood Pressure Monitor BPM25 & BPM26 Series [Model No.: MD25x0/ MD26x0]
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304239012·
Oticon
FDA UDI
Oticon A/S·05707131287045·H11V2, RITE 312 WL TC
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962104347·RAPIDCUT BLADE, 4.5MM, COMPATIBLE W/SN
UNICAP UNICOMPARTMENTAL KNEE RESURFACING PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
TYCHE PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962102350·DISPOSABLE ARTHROSCOPIC 4.5mm RAPIDCUT SHAVER B...
HEMICAP/UNICAP RESURFACING PROSTHESIS
FDA Adverse Event
Other
·ARTHROSURFACE, INC.·Product code HSD·December 7, 2012
VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT
FDA Adverse Event
Injury
·COOK VASCULAR INC·Product code LJT·January 7, 2016
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 25, 2024
TOTALCARE BARIATRIC PLUS BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·May 31, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 7, 2014
PROPEX
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code LQY·June 7, 2011
VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT
FDA Adverse Event
Malfunction
·COOK VASCULAR INC·Product code LJT·January 3, 2019
VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT
FDA Adverse Event
Malfunction
·COOK VASCULAR INC·Product code LJT·January 3, 2019
ORTHOPEDIC SALVAGE SYSTEM AXLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 17, 2017
ORTHOPEDIC SALVAGE SYSTEM (OSS) YOKE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·July 21, 2017
ORTHOPEDIC SALVAGE SYSTEM LOCKING PIN
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 17, 2017