10,000 results
·
100ms
·
Sources: EU EUDAMED, US FDA
NUCLEOSS
Device
EU MDD
·
Eu Md Class 2b
·Sanlilar Tibbi Cihazlar Med. Kim. San. Tic. Ltd. Sti·On the market·2 countries
NUCLEOSS
Device
EU MDD
·
Eu Md Class 2b
·Sanlilar Tibbi Cihazlar Med. Kim. San. Tic. Ltd. Sti·On the market·2 countries
NUCLEOSS
Device
EU MDD
·
Eu Md Class 2b
·Sanlilar Tibbi Cihazlar Med. Kim. San. Tic. Ltd. Sti·On the market·2 countries
NUCLEOSS
Device
EU MDD
·
Eu Md Class 2b
·Sanlilar Tibbi Cihazlar Med. Kim. San. Tic. Ltd. Sti·On the market·2 countries
NTM-Cera
Device
EU MDD
·
Eu Md Class 3
·Zesa Tıbbi Cihazlar Med. Kim. San. Tic. Ltd. Şti·On the market·1 country
NTM-Cera
Device
EU MDD
·
Eu Md Class 3
·Zesa Tıbbi Cihazlar Med. Kim. San. Tic. Ltd. Şti·On the market·1 country
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·INSYNC III (MODEL 9981 V8.0)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK(R) PRX(R) AICD(TM) SYSTEM FOR PECTORAL REPLACEMENT OF VENTAK PRXIII PULE GENERATOR
COOK
FDA UDI
William Cook Europe ApS·00827002236462·
Frova
FDA UDI
COOK INCORPORATED·00827002125919·Frova Intubating Introducer With Stiffening Can...
Cook
FDA UDI
COOK INCORPORATED·00827002221437·Double Lumen Wire Guided Billroth II Sphinctero...
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·APS III MODEL 3500 PROGRAMMER
Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring
FDA Pre-Market Approval
FDA Class 3
·AngioSculpt® Evo RX PTCA Scoring Balloon Catheter with Hydrophilic Coating
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·GEM MODEL 7227 ICD
FDA Pre-Market Approval
GEM III VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR(ICD)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 2490A CARELINK MONITOR AND DEVICE DATA MANAGEMENT APPLICATION (DDMA) SOFTWARE MODEL 2491 VERSION 1.0
FDA Pre-Market Approval
MEDTRONIC GEMIII DR MODEL 7275 (ICD), MODEL 9970 PROGRAMMER APPLICATION SOFTWARE
GT5 conductive & abrasive gel
FDA registration
WUHAN GREENTEK PTY LTD.·1 product·🇨🇳 China
Disposable EEG Electrodes (MODEL: DL, E-CAP, FLEX-CAP)
FDA registration
WUHAN GREENTEK PTY LTD.·1 product·🇨🇳 China