10,000 results · 100ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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