56 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AMPLATZER TORQVUE 45X45 DELIVERY SHEATH AMPLATZER TORQVUE LA1 DELIVERY SHEATH AMPLATZER TORQVUE LA2 SELIVERY SHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
AMPLATZER TORQVUE DELIVERY SYSTEM
FDA Adverse Event
Injury
·AGA MEDICAL CORPORATION·Product code DQY·July 3, 2012
Unity Total Knee System
FDA UDI
CORIN LTD·05056139243400·UNITY KNEE™ PS-C INSERT - Size 1 x 20mm
GENESIS 120 / 120 W
FDA UDI
NARVA Lichtquellen GmbH + Co KG.·04014501000083·
Aztec
FDA UDI
Aztecmed/Ent LLC·B87111201200·Klinik Nasal Speculum Medium
Life Instruments
FDA UDI
Life Instrument Corporation·M930712012010·American Rainbow Curette #2/0 Ang Red
Life Instruments
FDA UDI
Life Instrument Corporation·M930712012020·American Rainbow Curette #2/0 Rev Ang Red
Life Instruments
FDA UDI
Life Instrument Corporation·M93071201201C0·Custom #2/0 Curette slight angle
RIVA Pedicle Screw System
FDA UDI
XENIX MEDICAL LLC·00840493418711·CONSTRAINED LORDOTIC ROD, 5.5mm x 120mm
Life Instruments
FDA UDI
Life Instrument Corporation·M930712012000·American Rainbow Curette #2/0 Str Red
RIVA Pedicle Screw System
FDA UDI
XENIX MEDICAL LLC·00840493418926·CONSTRAINED LORDOTIC ROD, 6.0mm x 120mm
ENDOVIVE INITIAL PLACEMENT DIRECT PEJ KIT, ENDOVIVE STANDARD PROFILE BALLOON REPLACEMENT, MODELS 6520, 6521, 6220
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ALEXIS ORTHOPAEDIC WOUND RETRACTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Life Instruments
FDA UDI
Life Instrument Corporation·M9307120120240·Custom American Rainbow Curette #2/0 REV ANG 90...
Life Instruments
FDA UDI
Life Instrument Corporation·M9307120120220·Custom American Rainbow Curette #2/0 REV ANG 45...
Life Instruments
FDA UDI
Life Instrument Corporation·M9307120120110·American Rainbow Curette #2/0 Ang Red Custom
Life Instruments
FDA UDI
Life Instrument Corporation·M9307120120230·Custom American Rainbow Curette #2/0 REV ANG 90...
Life Instruments
FDA UDI
Life Instrument Corporation·M9307120120210·Custom American Rainbow Curette #2/0 REV ANG 45...
BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER WITH BLOOD CONTROL
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 15, 2017
PSI 120 120 40 PEEK
FDA Adverse Event
Malfunction
·Product code GXN·September 26, 2011