31 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CLEARFIL CERAMIC PRIMER PLUS, CLEARFIL CERAMIC PRIMER PLUS (Trial)
FDA 510(k)
FDA Class 2
·Dental
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768475·GENUMEDI PSS GREEN III
Oticon
FDA UDI
Oticon A/S·05707131280701·NERA2 PRO, BTE 13 WL 100 CBE
Healthweigh
FDA UDI
Rice Lake Weighing Systems, Inc.·00850042373569·Scale,Wheelchair Model RL-350-5 1000lb(450kg)x0...
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171028604·PESSARY, HODGE #0, W/O SUPPORT, 65mm
TELEFLEX
FDA UDI
TELEFLEX INCORPORATED·14026704713834·White Blue Co-braid Polyethylene Size 0 20" HR1...
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100189·MCINTYRE SPECULUM CLOSED WIRE
BLUESTITCH
FDA UDI
TELEFLEX INCORPORATED·14026704626509·White Blue Co-braid Polyethylene Size 0 20" HR1...
BLUESTITCH
FDA UDI
TELEFLEX INCORPORATED·44026704626500·White Blue Co-braid Polyethylene Size 0 20" HR1...
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE
STATIONARY X-RAY SYSTEM (DETECTOR) MODEL: ALTAS
FDA 510(k)
FDA Class 2
·Radiology
QBRAIN
FDA 510(k)
FDA Class 2
·Radiology
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·December 30, 2011
AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FNG·October 1, 2012
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·March 29, 2012
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·December 30, 2011
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·March 28, 2012
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code CAW·December 20, 2012
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·September 23, 2012