350 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
IFA SENSIBAC STREPTOMYCIN
FDA 510(k)
FDA Class 2
·Microbiology
ARiX RAD Radiographic System
FDA 510(k)
FDA Class 2
·Radiology
IFA SENSIBAC CEFACLOR
FDA 510(k)
FDA Class 2
·Microbiology
HEARTSCAN SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
VAPOCIDE
FDA 510(k)
FDA Class 2
·General Hospital
MARK IV FLOATATION THERAPY BED
FDA 510(k)
FDA Class 2
·Physical Medicine
DOCTORS REVIEW SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Anti-Mutated Citrullinated Vimentin Igg
FDA classification
FDA Class 2
·Anti-Mutated Citrullinated Vimentin Igg
AURORA SYSTEM 1000 SERIES HOME SELF-CARE SINGLE PATIENT DELIVERY SYSTEM; MODELS- SYS 1000, L3 WITH N100 ARM, 4B SOFTWARE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BLOOD MONITOR PUMP WITH ULTRAFILTRATION CONTROLLER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX THREADED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·VISTA LORDOTIC INTERBODY FUSION CAGE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC DEVICE/RAY TFC UNITE DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC UNITE PRODUCT LINE