243 results · 18ms · Sources: EU EUDAMED, US FDA

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