61 results
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32ms
·
Sources: EU EUDAMED, US FDA
EMIT ST URINE METHADONE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
TWINFIX
FDA UDI
Stryker GmbH·07613153161868·Screwdriver, Cann. Cross-Slot-Blade
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955932397·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955931291·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955930195·Percutaneous Transluminal Angioplasty Balloon C...
NA
FDA UDI
Zimmer, Inc.·00889024102088·
NA
FDA UDI
Zimmer, Inc.·00889024102095·
DIGITAL DENTAL INTRA ORAL SENSOR, HDI 2000, HDI 2000A
FDA 510(k)
FDA Class 2
·Radiology
SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
Zimmer, Inc.·00889024074125·
NA
FDA UDI
Zimmer, Inc.·00889024074132·
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014
CARE ASSIST BED
FDA Adverse Event
Malfunction
·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·November 8, 2012
RESTORE RECHARGABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 15, 2010
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·PMMA SINGLE-PIECE POSTERIOR CHAMBER IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·IOL LENS MODEL GR1A
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·PMMA Single-Piece Posterior Chamber Intraocular Lens