179 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·CRYOCOR CRYOABLATION SYSTEM
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·CRYOCOR CRYOABLATION SYSTEM
EASYLIFE
FDA UDI
Respironics, Inc.·00606959001329·Large EasyLife Mask with Headgear, China
Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989025354·PREF.LING.ARCH NI-TI UP18 SZ2 PK/10
Humelock II Cemented Reversible Shoulder
FDA UDI
FX SOLUTIONS·03701037300237·HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEP...
Ø7.0 x 24mm x 50mm CANNULATED PARTIAL THREAD SCREW
FDA UDI
Osteocentric Technologies, Inc.·00816950026690·Ø7.0 x 24mm x 50mm CANNULATED PARTIAL THREAD SCREW
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710300500240·Tibial Osteotmy Guide, 50mm x 24mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710420500240·Anterior Lateral Wedge Osteotomy Guide, 50mm x ...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710400500240·Anterior Dome Osteotomy Guide, 50mm x 24mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710410500240·Anterior Closing Wedge Osteotomy Guide, 50mm x ...
ONE STEP MULTIPLE DRUGS OF ABUSE ASSAYS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PORTEX CO2 CLIP
FDA Adverse Event
Death
·SMITHS MEDICAL ASD, INC.·Product code CCK·November 9, 2005
HUMELOCK REVERSED SHOULDER
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·June 21, 2019
Qualitative And Quantitative Hepatitis B Virus Antibody Assays
FDA Pre-Market Approval
FDA Class 2
·VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC REAGENT PACK/CALIBRATOR
Occluder, Patent Ductus, Arteriosus
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER DUCT OCCLUDER AND 180 DEGREE DELIVERY SYSTEM
HUMELOCK REVERSED SHOULDER
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·July 9, 2019
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·April 13, 2012
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·May 16, 2008
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·March 29, 2007
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·April 14, 2011