2,371 results · 37ms · Sources: EU EUDAMED, US FDA

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·PulseSelect PFA Loop Catheter

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·Sphere-9™ Mapping and Ablation Catheter, Catheter Extension Cable, Tubing Set

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·Sphere-9 Catheter and Affera Ablation System

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·Sphere-9 Catheter and Affera Ablation System

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·VARIPULSE™ Platform (VARIPULSE™ Catheter; TRUPULSE™ Generator; Sterile Interface Cable; nGEN™ Pump)

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·PulseSelect™ Pulsed Field Ablation (PFA) system

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·FARAPULSE™ Pulsed Field Ablation System (FARAWAVE™ Pulsed Field Ablation Catheter, FARAWAVE™ NAV Pulsed Field Ablation C

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval
FDA Class 3 ·FARAPULSE™ Pulsed Field Ablation System (FARAWAVE™ Pulsed Field Ablation Catheter, FARASTAR™ Catheter Connection Cable,

NA

FDA UDI
Hangwei GE Medical Systems Co., Ltd.·00840682141932·

Bordetella Direct Test

FDA UDI
GREAT BASIN SCIENTIFIC, INC.·B178GBBORD100·Bordetella Direct Test Cartridge

REAL RESPIRATORY BACTERIAL PANEL 2 (B. pertussis, B. parapertussis, B. holmesii) (Code/código: 5.182.XXX.88.ZZZ)

Device
EU IVDR · Eu Ivd Class B ·OPERON, S.A.·On the market·1 country

SET ZZ BASE ZZ-MUA-WSM OP

FDA UDI
ZIRKONZAHN SRL·D800ZBCD9233·SET ZZ BASE ZZ-MUA-WSM OP (White Scanmarker and...

SET ZZ BASE ZZ-MUA-WSM SP

FDA UDI
ZIRKONZAHN SRL·D800ZBCD9232·SET ZZ BASE ZZ-MUA-WSM SP (White Scanmarker and...

Screwdriver ZZ MUA

FDA UDI
ZIRKONZAHN SRL·D800SIAK2001·Screwdriver ZZ MUA - Screw driver to fix non-an...

ZZ BASE ZZ-MUA-ICSC (Impression coping Screw)

FDA UDI
ZIRKONZAHN SRL·D800BSFE9201·Compatible with Zirkonzahn Multi Unit Abutment ...

ZZ BASE ZZ-LO-WSM 3.86 (White Scanmarker)

FDA UDI
ZIRKONZAHN SRL·D800ZBCD10431·Compatible with Zirkonzahn Locator Set consist...

ZZ BASE ZZ-MUA-ICSC OP (Impression coping Screw)

FDA UDI
ZIRKONZAHN SRL·D800BSFE9203·Compatible with Zirkonzahn Multi Unit Abutment ...

ZZ BASE ZZ-MUA-ICSC SP (Impression coping Screw)

FDA UDI
ZIRKONZAHN SRL·D800BSFE9202·Compatible with Zirkonzahn Multi Unit Abutment ...

K-Z Z-TURN

FDA UDI
KAP MEDICAL·00817012023640·K-Z Alternating Rotation, True Low Air Loss, Ba...

K-Z Z-TURN

FDA UDI
KAP MEDICAL·00817012030136·Auto Immerssion, Alternating Rotation, Pulsatio...