23 results · 43ms · Sources: EU EUDAMED, US FDA

518-043 7 Fr TURBO BOOSTER

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

7 Fr TURBO BOOSTER

FDA registration
Terumo BCT STERILIZATION SERVICES, Inc.·1 product·🇺🇸 United States

8FR TURBO BOOSTER, GUIDE CATHETER, 7FR TURBO BOOSTER, MODEL 518-063, 518-043

FDA 510(k)
FDA Class 2 ·Cardiovascular

Catheter For Crossing Total Occlusions

FDA classification
FDA Class 2 ·Catheter For Crossing Total Occlusions

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526780781·LEVAMED ACTIVE ANKLE SUP SLVR L VI

Zimmer (Shanghai) Medical International Trading Co., Ltd.

FDA registration
Zimmer (Shanghai) Medical International Trading Co., Ltd.·1 product·🇨🇳 China

Zimmer (DK) - TRABECULAR METAL ACETABULAR REVISION SYSTEM CAGE

FDA registration
Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

Trabecular Metal Acetabular Revision System Cage

FDA registration
Zanol GmbH·1 product·🇨🇭 Switzerland

Synergy Health Sterilisation UK Ltd

FDA registration
Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom

ZIMMER PTE. LTD.

FDA registration
ZIMMER PTE. LTD.·1 product·🇸🇬 Singapore

Actifuse ABX

FDA registration
APATECH LTD.·1 product·🇬🇧 United Kingdom

TM Acetabular Revision Sys. Cage

FDA registration
ZIMMER, INC.·1 product·🇺🇸 United States

Actifuse ABX

FDA registration
BAXTER HEALTHCARE CORPORATION·1 product·🇺🇸 United States

TRABECULAR METAL ACETABULAR REVISION SYSTEM CAGE

FDA registration
Sterigenics US, LLC·1 product·🇺🇸 United States

Trabecular Metal Acetabular Revision

FDA registration
ZIMMER GMBH·1 product·🇨🇭 Switzerland

Trabecular Metal Acetabular Revision

FDA registration
Biomet Global Supply Chain Center B.V.·1 product·🇳🇱 Netherlands

Zimmer Biomet Pty Ltd

FDA registration
Zimmer Biomet Pty Ltd·1 product·🇦🇺 Australia

Infusor SV & LV Elastomeric Infusion Devices

FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States

KATMAI INTEGRATED SOLUTIONS

FDA registration
KATMAI INTEGRATED SOLUTIONS·1 product·🇺🇸 United States

SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic