Meridius Medical Europe Limited

Authorized representative

🇮🇪 Ireland·36 Manufacturers·720 Devices

Biomet® Knee System

FDA UDI

Biomet Orthopedics, LLC·00887868344336·

BIOMET KNEE SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304009653·

BIOMET KNEE SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304006843·

Biomet® Knee System

FDA UDI

Biomet Orthopedics, LLC·00887868344329·

BIOMET KNEE SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304002432·

Biomet® Knee System

FDA UDI

Biomet Orthopedics, LLC·00887868344343·

Vanguard Knee System

FDA UDI

Biomet Orthopedics, LLC·00880304435025·

AGC Knee System

FDA UDI

Biomet Orthopedics, LLC·00880304243057·

Berner Oy

Importer

🇫🇮 Finland·16 Manufacturers

System, Balloon, Intra-Aortic And Control, Reprocessed

FDA classification

FDA Class 3 ·System, Balloon, Intra-Aortic And Control, Reprocessed

Catheter, Oximeter, Fiber Optic, Reprocessed

FDA classification

FDA Class 2 ·Catheter, Oximeter, Fiber Optic, Reprocessed

Trocar, Reprocessed

FDA classification

FDA Class 2 ·Trocar, Reprocessed

Bur, Diamond Coated, Reprocessed

FDA classification

FDA Class 1 ·Bur, Diamond Coated, Reprocessed

Biopsy Device, Percutaneous, Reprocessed

FDA classification

FDA Class 1 ·Biopsy Device, Percutaneous, Reprocessed

Needle And Needle Set, Gastro-Urology, Reprocessed

FDA classification

FDA Class 2 ·Needle And Needle Set, Gastro-Urology, Reprocessed

Needle, Biopsy, Cardiovascular, Reprocessed

FDA classification

FDA Class 1 ·Needle, Biopsy, Cardiovascular, Reprocessed

Catheter, Steerable, Reprocessed

FDA classification

FDA Class 2 ·Catheter, Steerable, Reprocessed

Needle, Dental, Reprocessed

FDA classification

FDA Class 1 ·Needle, Dental, Reprocessed

Needle, Aspiration And Needle, Reprocessed

FDA classification

FDA Class 1 ·Needle, Aspiration And Needle, Reprocessed