10,000 results
·
56ms
·
Sources: EU EUDAMED, US FDA
Peripheral Balloon Expandable Stent System (QBX)
Device
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·On the market·1 country
Peripheral Balloon Expandable Stent System (QBX)
Device
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·On the market·1 country
THE TRABECULAR METAL MONOBLOCK CUP, MODELS 00-7259-0XX-28 (ZIMMER CAT. #) AND 02-293-28XX1 (IMPLEX PART #)
FDA 510(k)
FDA Class 2
·Orthopedic
Dental Implant Unit
FDA 510(k)
FDA Class 1
·Dental
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·THERMOCOOL SF NAV BI-DIRECTIONAL CATHETER (D1313-XX-S, D-1317-XX-S) AND THERMOCOOL SF BI-DIRECTIONAL CATHETER
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·THERMOCOOL SF NAV BI-DIRECTIONAL CATHETER (D-1313-XX-S, D-1317-XX-S) AND THERMOCOOL SF BI-DIRECTIONAL CATHETER
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·THERMOCOOL SF NAV UNI-DIRECTIONAL CATHETER (D-1315-XX-S, D-1318-XX-S) AND THERMOCOOL SF UNI-DIRECTIONAL CATHETER
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·THERMOCOOL SF NAV UNI-DIRECTIONAL CATHETER (D-1315-XX-S, D-1318-XX-S) AND THERMOCOOL SF UNI-DIRECTIONAL CATHETER
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·BI-DIRECTIONAL CELSIUS FLTR CATHETERS (D-1359-XX-S)
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·UNI-DIRECTIONAL CELSIUS FLTR CATHETERS (D-1355-XX S)
INSPEKTOR PRO
FDA 510(k)
FDA Class 2
·Dental
Maris Care Slip met Plakstrip Super L
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Maris Care BV·1 device
Atlas Surgical and Prosthetic Instrumentation Kit
FDA UDI
Dentatus AB·07350081494872·ATLAS Surgical and Prosthetic Instrumentation k...
neos
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·machineMD AG·1 device
13 QBX 060175F
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·1 device
13 QBX 070265F
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·1 device
13 QBX 050575F
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·1 device
13 QBX 050365F
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·1 device
13 QBX 070175F
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·1 device
13 QBX 060365F
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·QualiMed Innovative Medizinprodukte GmbH·1 device