21 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Tech Industries. Inc.
FDA registration
Tech Industries. Inc.·2 products·🇺🇸 United States
ZAVATION IBF SYSTEM
FDA registration
ZAVATION·2 products·🇺🇸 United States
ZAVATION IBF SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SYNTHES USS CONNECTOR; K120571
FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·5 products·🇺🇸 United States
D/Sense Crystal
FDA registration
CENTRIX, INC.·1 product·🇺🇸 United States
High Pressure Sets
FDA registration
ICU MEDICAL DE MEXICO, S. de R.L. de C.V.·1 product·🇲🇽 Mexico
Isomedix Operations, Inc
FDA registration
Isomedix Operations, Inc·1 product·🇺🇸 United States
High Pressure Sets
FDA registration
ICU MEDICAL, INC·1 product·🇺🇸 United States
Set, administration, intravascular
FDA registration
Medline Industries, LP - Mexicali (MXC)·1 product·🇲🇽 Mexico
TRI-STATE DE MEXICO, S. DE R.L. DE C.V.
FDA registration
TRI-STATE DE MEXICO, S. DE R.L. DE C.V.·1 product·🇲🇽 Mexico
Administration Sets and Accessories
FDA registration
Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States
Set, administration, intravascular
FDA registration
MEDLINE INDUSTRIES, LP (Northpoint Services)·1 product·🇺🇸 United States
BioPlex 2200 ToRC IgM kit
FDA registration
Bio-Rad Laboratories, Inc.·3 products·🇺🇸 United States
MEVION S250 Proton Therapy System
FDA registration
MEVION MEDICAL SYSTEMS, INC.·1 product·🇺🇸 United States
IMMULITE 2000 Anti-CCP Calibration Verification Material
FDA registration
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·2 products·🇬🇧 United Kingdom
BioPlex2200 ToRC IgG Reagent Pack
FDA registration
BIO-RAD LABORATORIES, INC.·3 products·🇺🇸 United States
VELOGENE GENOMIC IDENTIFICATIONASSAY FOR VRE
FDA 510(k)
FDA Class 2
·Microbiology
HIGH PRESSURE SETS-400 PSI
FDA 510(k)
FDA Class 2
·General Hospital
System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species
FDA classification
FDA Class 2
·System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar