622 results
·
52ms
·
Sources: EU EUDAMED, US FDA
ZERAMEX® WB Gingivaformer, 4mm
FDA UDI
Dentalpoint AG·07640161392243·Prosthetics
ZERAMEX® WB Healing Cap
FDA UDI
Dentalpoint AG·07640161392229·Prosthetics
ZERAMEX® WB Implant Replica
FDA UDI
Dentalpoint AG·07640161392601·Acessories
ZERAMEX® WB Transfer Closed Tray, long
Device
EU MDR
·
Eu Md Class 1
·CeramTec Schweiz GmbH·On the market
SC MTUBE,2ML,PP,CBS,GWB
FDA UDI
Sarstedt Aktiengesellschaft & Co.KG·04038917926386·
ZERAMEX® WB Transfer Open Tray
FDA UDI
Dentalpoint AG·07640161392489·Acessories
ZERAMEX® WB Transfer Closed Tray
FDA UDI
Dentalpoint AG·07640161392502·Acessories
ZERAMEX® WB Provisional (incl. Screw)
FDA UDI
Dentalpoint AG·07640161392250·Prosthetics
SC MTUBE,2ML,BROWN,CBS,GWB
FDA UDI
Sarstedt Aktiengesellschaft & Co.KG·04038917926423·
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REVO MRI IPG
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EVERA S DR ICD,EVERA S VR ICD,EVERA XT DR ICD,EVERA XT VR ICD, MAXIMO II ICD, PROTECTA ICD, PROTECTA XT ICD, SECURA ICD
FDA Pre-Market Approval
BRAVA CRT-D,CONCERTO II CRT-D,CONSULTA ICD,MAXIMO II CRT-D,PROTECTA CRT-D,PROTECTA XT CRT-D,VIVA S CRT-D
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·CONSULTA CRT-P, SYNCRA CRT-P
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·ADAPTA,VERSA,SENSIA IPG, ADVISA DR IPG,ADVISA DR MRI IPG,RELIA IPG
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra XT SR MRI IPG, Azure S DR MRI IPG, Azure S SR MRI IPG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Solara Bipolar CRT-P
Leadless Pacemaker
FDA Pre-Market Approval
FDA Class 3
·Micra AV TPS, Micra TPS, Micra VR TPS
SURGICAL GLOVES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CATHETER, CARDIOVASCULAR, BALLOON TYPE
FDA 510(k)
FDA Class 2
·Cardiovascular
RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R
FDA 510(k)
FDA Class 2
·Neurology