243 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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NEPHROS, INC., DSU DUAL STAGE ULTRAFILTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EndoPur Filter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NEPHROS OLPUR H2H HEMODIAFILTRATION (HDF) MODULE AND OLPUR MD 220 HEMODIAFILTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HydraGuard 10 UltraFilter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NEPHROS DSU-H, NEPHROS SSU-H
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POS-T-VAC (IVP-600)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SUPPORT SLEEVE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BOSS-2000-2 VACUUM ERECTION DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POS-T-VAC (AVP-1000)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LT-CAGE TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK VISTA INTERBODY FUSION DEVICE
GPC Intramedullary Nailing Systems
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM
Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)
FDA Pre-Market Approval
FDA Class 2
·MICRO-PACE MODEL 4553 DUAL CHAMBER DDD TEMPORARY CARDIAC PACEMAKER
Pulse-Generator, Pacemaker, External
FDA Pre-Market Approval
FDA Class 2
·MICRO-PACE MODEL 4580 DUAL-CHAMBER,DDD,TEMPORARY CARDIAC PACEMAKER
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LORDOTEC(TM) TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK VISTA INTERBODY FUSION CAGE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC DEVICE AND RAY TFC UNITE DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BRANTIGEN I/F CAGE(R) USED WITH VSP(R) SPINE PLATES AND PEDICLE SCREWS