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