10,000 results
·
426ms
·
Sources: EU EUDAMED, US FDA
Digital Breast Tomosynthesis
FDA Pre-Market Approval
FDA Class 3
·ASPIRE CRISTALLE DIGITAL BREAST TOMOSYNTHESIS OPTION
POLYFLUX
FDA UDI
Gambro Dialysatoren GmbH·07332414031787·Polyflux R is intended for use in hemodialysis ...
RXEars
FDA UDI
Persona Medical·00851362008322·Hearing Device incorporating an adjustable push...
TelePatch Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000388·TelePatch CM PM750 is a small, auto triggered, ...
POLYFLUX
FDA UDI
Gambro Dialysatoren GmbH·07332414031770·Polyflux R is intended for use in hemodialysis ...
POLYFLUX
FDA UDI
Gambro Dialysatoren GmbH·07332414036140·Polyflux R is intended for use in hemodialysis ...
Titan
FDA UDI
TITAN MANUFACTURING INC·00817914024141·Blue Titanium Round Handle Bayonet Bipolar Forc...
Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000357·Cardiac Monitor PM500 is a small, auto triggere...
TelePatch Cardiac Monitor
FDA UDI
MEDICOMP, INC.·00862887000371·TelePatch CM PM700 is a small, auto triggered, ...
Provox Silicone Glue
FDA UDI
Atos Medical AB·07331791002984·Provox Silicone Glue is a liquid glue used for ...
Titan
FDA UDI
TITAN MANUFACTURING INC·00817914020280·Nadler Style Coaptation Bipolar Forcep With Rem...
Titan
FDA UDI
TITAN MANUFACTURING INC·00817914023076·Blue Titanium M-Style Square Grip Handle Bayone...
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·IPRO2 CGM SYSTEM WITH ENLITE SENSOR
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·HYDROGENICS 2.0 UV ASPHERE (OCUFILCON F) SOFT (HYDROPHILIC) CONTACT LENS FOR EXTENDED WEAR
Integra Spetzler™ Lumbar Peritoneal Shunt System
FDA UDI
Integra Lifesciences Corporation·10381780072539·LONG SPETZLER 105CM LP SHUNT
The Spetzler Lum...
RP Low Margin Abutment Plastic Cylinder, 8.0 mm
FDA UDI
STERNGOLD DENTAL LLC·00841549111204·A prefabricated device intended to provide a pe...
ORA Retaining Ring
FDA UDI
STERNGOLD DENTAL LLC·00841549110139·ORA Retaining Ring. The ORA Implant Abutment S...
System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex
FDA Pre-Market Approval
FDA Class 2
·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·Gore Excluder AAA Endoprosthesis and Gore Excluder Iliac Branch Endoprosthesis
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·PHILOS DR-T PULSE GENERATOR/ICD BELOS VR-T,DR-T,ICD CARDIAC AIRBAG-T