73 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACON COMBO PREGNANCY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ICON 25 HCG (COMBO CASSETTE)
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code JHI·March 16, 2017
artegral life
FDA UDI
Merz Dental GmbH·D7091993065·anteriors; shade A2; mould UBIS
SCOTT'S HANDHELD AUTOMIX CORE 2/pk BLUE
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77819930651·
PRIMARY MANUFACTURER SUNGLASSES
FDA 510(k)
FDA Class 1
·Ophthalmic
FINESSE PERSONAL INSULIN DELIVERY PATCH, MODEL FG-2000
FDA 510(k)
FDA Class 2
·General Hospital
HOMECHOICE, DOMESTIC 120V
FDA Adverse Event
BAXTER HEALTHCARE·Product code FKX·June 11, 2008
HOMECHOICE, DOMESTIC 120V
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·July 24, 2009
PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 18, 2008
HOMECHOICE CYCLER-REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·December 4, 2007
HOMECHOICE CYCLER-REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·December 10, 2007
PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 18, 2008
PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 27, 2008
PD CYCLER 110 VOLT HOME CHOCIEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 18, 2008
PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 18, 2008
HOMECHOICE CYCLER-REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 13, 2008
HOMECHOICE CYCLER -REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 5, 2008
HOMECHOICE CYCLER REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·March 6, 2008
HEMA 4 BRANCH 20MM PLATINUM GRAFT
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DSY·March 1, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 8, 2011