2,427 results · 48ms · Sources: EU EUDAMED, US FDA

Nasal Cannula

Basic UDI-DI
EU MDR · Eu Md Class 2a ·Ningbo Shengyurui Medical Appliances Co., Ltd.·23 devices

SIGNA Premier

Basic UDI-DI
EU MDR · Eu Md Class 2a ·GE Medical Systems LLC·1 device

Nasal Cannula

Basic UDI-DI
EU MDR · Eu Md Class 2a ·Ningbo Shengyurui Medical Appliances Co., Ltd.·96 devices

Needle-Free Valve Port

Basic UDI-DI
EU MDD · Eu Md Class 2a ·ASSET MEDIKAL TASARIM SANAYI VE TICARET ANONIM SIRKETI·1 device

SIGNA Pioneer

Basic UDI-DI
EU MDR · Eu Md Class 2a ·GE Medical Systems LLC·1 device

SIGNA Hero

Basic UDI-DI
EU MDR · Eu Md Class 2a ·GE Medical Systems LLC·1 device

Permanent Pacemaker Electrode

FDA Pre-Market Approval
FDA Class 3 ·TENDRIL DX MODEL 1388T & 1388K ENDOCARDIAL PACING LEADS

Implant, Cochlear

FDA Pre-Market Approval
FDA Class 3 ·HiResolution Bionic Ear System

Phlecs full body blue

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Phlecs B.V.·1 device

Mr-Guided Focused Ultrasound System

FDA Pre-Market Approval
FDA Class 3 ·Exablate Model 4000 Type 1.0 and 1.1 Systems (“Exablate Neuro”)

Permanent Pacemaker Electrode

FDA Pre-Market Approval
FDA Class 3 ·PASSIVE PLUS DX STEROID ELUTING, ENDOCARDIAL PACING LEADS

Stimulator, Invasive Bone Growth

FDA Pre-Market Approval
FDA Class 3 ·EBI OSTEOGEN BONE GROWTH IMPLANTABLE BONE GROWTH STIMULATOR

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·SPRINT QUATTRO SECURE S SINGLE COIL IS-1/DF-1, ACTIVE FIX LEAD MODEL 6935

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·cobas HPV TEST

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·cobas HPV for use on the cobas 6800/8800 Systems

Intracranial Coil-Assist Stent

FDA Pre-Market Approval
FDA Class 3 ·Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.

Roche farmacevtska družba d.o.o.

Importer
🇸🇮 Slovenia

HDL UNION SRL

Importer
🇷🇴 Romania·4 Manufacturers

Ridian AS

Importer
🇳🇴 Norway

Agent, Bulking, Injectable For Gastro-Urology Use

FDA Pre-Market Approval
FDA Class 3 ·DURASPHERE INJECTABLE BULKING AGENT