GC Initial™

FDA UDI

Gc America Inc.·J0228725401·GC Initial™ IQ/Correction Powder A1-M, 5g

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215027·5F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215034·4F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333214990·4F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215058·4F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215041·5F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215065·5F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215003·5F Percutaneous Micro-Introducer Kit

Percutaneous Micro-Introducer Kit

FDA UDI

ARGON MEDICAL DEVICES, INC.·00886333215010·4F Percutaneous Micro-Introducer Kit

GC Initial™

FDA UDI

Gc America Inc.·J0228725491·GC Initial™ IQ/Correction Powder Bleach BOO-M, 5g

GC Initial™

FDA UDI

Gc America Inc.·J0228725471·GC Initial™ IQ/Correction Powder Bleach AO-M, 5g

GC Initial™

FDA UDI

Gc America Inc.·15400556709495·GC Initial™ IQ/Correction Powder Bleach BO-M, 5g

GC Initial™

FDA UDI

Gc America Inc.·15400556709488·GC Initial™ IQ/Correction Powder Bleach AO-M, 5g

GC Initial™

FDA UDI

Gc America Inc.·15400556709501·GC Initial™ IQ/Correction Powder Bleach BOO-M, 5g

GC Initial™

FDA UDI

Gc America Inc.·J0228725481·GC Initial™ IQ/Correction Powder Bleach BO-M, 5g

Mag-Plates

Device

EU IVDR · Eu Ivd Class A ·DIAGAST·On the market·6 countries

MAG GYM

Device

EU MDR · Eu Md Class 2a ·Iskra Medical, d.o.o., raziskave in razvoj na področju medicinske opreme in kozmetike·On the market·32 countries

UNI MAG TIBBİ VE KİMYASAL MALZEMELER SAN. VE TİC. LTD. ŞTİ.

Manufacturer

🇹🇷 Türkiye

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval

FDA Class 3 ·Multifunctional Ablation Generator (MAG)

Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval

FDA Class 3 ·Multifunctional Ablation Generator (MAG)