CPS Direct Universal Slittable Outer Guide Catheter (Redesign) (DS2C029)

FDA registration

ABBOTT MEDICAL·1 product·🇺🇸 United States

CPS Direct™ Universal slittable outer guide catheter (DS2C029)

FDA 510(k)

FDA Class 2 ·Cardiovascular

BD BBL™ Sensi-Disc™ Nalidixic Acid - 30 µg

FDA UDI

BECTON, DICKINSON AND COMPANY·30382902313114·BD BBL™ Sensi-Disc™ Nalidixic Acid 30 µg

CC3050-L

FDA registration

JEIL MEDICAL CORPORATION·1 product·🇰🇷 South Korea

CC3050-L

FDA registration

JEIL MEDICAL CORPORATION·1 product·🇰🇷 South Korea

ARIX Foot System

FDA registration

MAXXHEALTH·1 product·🇺🇸 United States

PF4 IgG assay

FDA registration

Immucor GTI Diagnostics, Inc.·1 product·🇺🇸 United States

Intrigue

FDA UDI

LANCER ORTHODONTICS, INC.·00817573021550·INTRG WHISP MBT LAT +10T +8A 022 UR

TP Original Wire

FDA UDI

TP ORTHODONTICS INC·00192029028810·Standard Plus Round

Merilas 810 shortpulse

FDA registration

MERIDIAN AG·1 product·🇨🇭 Switzerland

Diode Laser Body Sculpture Systems

FDA registration

SHANGHAI BELE MEDICAL TECHNOLOGY CO.,LTD·1 product·🇨🇳 China

ComfortTemp

FDA registration

CAREMED SUPPLY, INC.·1 product·🇹🇼 Taiwan

X SERIES

FDA UDI

Zoll Medical Corporation·00847946020132·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

X SERIES

FDA UDI

Zoll Medical Corporation·00847946023553·DEVICE IDENTIFIER,X SERIES MONITOR/DEFIBRILLATO...

TALOS® HA PEEK IBF

FDA UDI

MEDITECH SPINE, LLC·B167322313110·

X SERIES

FDA UDI

Zoll Medical Corporation·00847946062088·X SERIES MONITOR/DEFIBRILLATOR 12 LEAD/W INTERP...

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167312313110·

ARIX FOOT SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

INTEGRADWEB BY DYNAMIC IMAGING, INC.

FDA 510(k)

FDA Class 2 ·Radiology

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous