Reprocessed Transseptal Needle

FDA registration

INNOVATIVE HEALTH, LLC.·1 product·🇺🇸 United States

Reprocessed NRG Transseptal Needle

FDA 510(k)

FDA Class 2 ·Cardiovascular

Septostomy Catheter, Reprocessed

FDA classification

FDA Class 2 ·Septostomy Catheter, Reprocessed

Stainless Steel Angiography Guide Wires

FDA registration

Sterigenics U.S., LLC·3 products·🇺🇸 United States

Stainless Steel Angiography Guide Wires

FDA registration

Sterigenics U.S., LLC·3 products·🇺🇸 United States

Stainless Steel Angiography Guide Wires

FDA registration

Sterigenics US LLC·3 products·🇺🇸 United States

Stainless Steel Angiography Guide Wires

FDA registration

Sterigenics U.S., LLC·3 products·🇺🇸 United States

RIVERSIDE MACHINE & ENGINEERING, INC.

FDA registration

RIVERSIDE MACHINE & ENGINEERING, INC.·3 products·🇺🇸 United States

PressureWire Certus Agile Tip

FDA registration

St. Jude Medical, Cardiology Division, Inc.·3 products·🇺🇸 United States

Wire, guide, catheterTRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCYTRANSDUCER, PRESSURE, CATHETER TIP

FDA registration

SUZHOU PROSTERI MEDICAL TECHNOLOGY CO., LTD.·3 products·🇨🇳 China

Metal Craft Machine & Engineering, Inc.

FDA registration

Metal Craft Machine & Engineering, Inc.·3 products·🇺🇸 United States

transducer, pressure, catheter tip

FDA registration

SHANGHAI JPY ION-TECH CO., LTD.·3 products·🇨🇳 China

Stainless Steel Angiography Guide Wires

FDA registration

Sterigenics Belgium Petit Rechain S.A.·3 products·🇧🇪 Belgium

Stainless Steel Angiography Guide Wires

FDA registration

Sterigenics U.S. LLC·3 products·🇺🇸 United States

transducer, pressure, catheter tip

FDA registration

SHANGHAI JPY ION-TECH CO., LTD.·3 products·🇨🇳 China

SYNGO, CT BONE READING

FDA registration

Siemens Healthineers AG·1 product·🇩🇪 Germany

BiWaze Clear System

FDA registration

AMT PTE. LTD.·1 product·🇸🇬 Singapore

MZ Skin LightMAX Supercharged LED Mask 2

FDA registration

I-SMART Development LTD.·2 products·🇬🇧 United Kingdom

PRESSUREWIRE CERTUS, CERTUS 300, AERIS, AERIS 300, AND RECEIVER

FDA 510(k)

FDA Class 2 ·Cardiovascular

EXCITE SELF ETCH

FDA 510(k)

FDA Class 2 ·Dental