31 results · 21ms · Sources: EU EUDAMED, 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