PERLA

FDA registration

SPINEART SA·2 products·🇨🇭 Switzerland

PERLA

FDA registration

COULOT DECOLLETAGE·2 products·🇫🇷 France

Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·2 products·🇨🇭 Switzerland

PERLA

FDA registration

Alpes CN·2 products·🇫🇷 France

PERLA

FDA registration

ALPES CN SAS·2 products·🇫🇷 France

PERLA

FDA registration

ALPES CN·2 products·🇫🇷 France

Perla Posterior Cervico-Thoracic Fixation system

FDA 510(k)

FDA Class 2 ·Orthopedic

Posterior Cervical Screw System

FDA classification

FDA Class 2 ·Posterior Cervical Screw System

AGC KNEE SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304222205·

EMU 40

FDA registration

NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD. (XLTEK)·1 product·🇨🇦 Canada

5F and 8F Launcher Guiding Catheter

FDA registration

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

CATHETER, PERCUTANEOUS

FDA registration

CARDIMED ASIA MEDIKAL SANAYI VE TICARET LTD STI·1 product·🇹🇷 Türkiye

EMU40

FDA registration

CREATION TECHNOLOGIES LTD·1 product·🇨🇦 Canada

5F and 8F Launcher Guiding Catheter

FDA registration

MEDTRONIC VASCULAR·1 product·🇺🇸 United States

XLTEK EMU40 EEG HEADBOX, MODEL PK1072

FDA 510(k)

FDA Class 2 ·Neurology

MEDTRONIC VASCULAR - HUB MATERIAL MODIFICATION TO THE 5F AND 8F LAUNCHER(R) GUIDE CATHETERS

FDA 510(k)

FDA Class 2 ·Cardiovascular

Full-Montage Standard Electroencephalograph

FDA classification

FDA Class 2 ·Full-Montage Standard Electroencephalograph

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous