105 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FOUNDATION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704289428·
Needle Holder
FDA UDI
KOROS U.S.A., INC.·10840199540386·Ryder Needle Holder 21cm 8-1/2"
STAGE IV, AIR-FLUIDIZE BED
FDA 510(k)
FDA Class 2
·Physical Medicine
ACCLAIM* BRACKET ADHESIVE
FDA 510(k)
FDA Class 2
·Dental
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
COMPOUNDERS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·October 27, 2012
COMPOUNDERS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·September 6, 2012
COMPOUNDERS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code NEP·August 10, 2012
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·February 15, 2013
MX-PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV.·Product code INK·January 12, 2011
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·July 9, 2014
COMPOUNDERS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·November 2, 2012