IMMULITE ACTH

FDA registration

Siemens Healthcare Diagnostics Inc.·1 product·🇺🇸 United States

IMMULITE ACTH

FDA registration

SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·1 product·🇬🇧 United Kingdom

IMMULITE ACTH

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

Radioimmunoassay, Acth

FDA classification

FDA Class 2 ·Radioimmunoassay, Acth

N/A

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994550804·LID 7960066 TRIAL CADDY

The Pro-Link Titanium System

FDA registration

LIFE SPINE·1 product·🇺🇸 United States

Reinfusion Bag 1000 mL

FDA registration

FENWAL, INC.·1 product·🇺🇸 United States

Pro Link Instruments

FDA registration

ZIBO DANTE CO, LTD·1 product·🇨🇳 China

Intervertebral fusion device with integrated fixation, cervical

FDA registration

Acero Precision·1 product·🇺🇸 United States

Reinfusion Bag 1000 mL

FDA registration

FRESENIUS HEMOCARE GMBH·1 product·🇩🇪 Germany

Pro-Link Orthopedic Manual Surgical Instrument

FDA registration

GIZMO PRECISION MEDICAL LLC·1 product·🇺🇸 United States

Titan Reverse Shoulder System

FDA UDI

Smith & Nephew, Inc.·00885556863923·GLENOSPHERE IMPACTOR MOD

VERIFY 3-10 MIN FLASH INTEGRATOR

FDA 510(k)

FDA Class 2 ·General Hospital

Pro-Link® Stand-Alone Cervical Spacer System

FDA 510(k)

FDA Class 2 ·Orthopedic

Titan™

FDA UDI

Ascension Orthopedics, Inc.·10381780245667·Titan™ Reverse Shoulder System Glenosphere Impa...

Intervertebral Fusion Device With Integrated Fixation, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Cervical

Indicator, Physical/Chemical Sterilization Process

FDA classification

FDA Class 2 ·Indicator, Physical/Chemical Sterilization Process