37 results
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20ms
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Sources: EU EUDAMED, US FDA
RDH BANDAGE
FDA 510(k)
FDA Class 1
·General Hospital
Bristol Holster
FDA UDI
LONG ISLAND TECH·00851610007275·Light & Surgical Accessory
Dover Holster
FDA UDI
LONG ISLAND TECH·00851610007268·
Essix A+
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D74610025501·Essix A+ .020 x 5" square 50PK
AirLife
FDA UDI
Carefusion Corporation·10885403039294·Airlife™ Misty Finity™ Small Volume...
AirLife™
FDA UDI
AIRLIFE·10889483571316·AirLife™ Misty Finity™ Small Volume Low Flow Co...
AirLife™
FDA UDI
VYAIRE MEDICAL, INC.·10190752156616·AirLife™ Misty Finity™ Small Volume Low Flow Co...
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361009245·PedFuse, Rod, Straight, Bulleted, 5.5mm X 50mm
Mariner MIS
FDA UDI
Seaspine Orthopedics Corporation·10889981171476·MIS Tap A/O, Dia 5.50mm
OTW MEGALINK SDS BILIARY STENT SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EBT ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-150LXP OR C-150XP SCANNER SYSTEMS; ELECTRON BEAM SCANNER SYSTEM; ELECTR
FDA 510(k)
FDA Class 2
·Radiology
HEMOVAC KIT
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code ILZ·August 31, 2004
RIVA Posterior Fixation System
FDA UDI
XENIX MEDICAL LLC·00840493418223·CONSTRAINED STRAIGHT ROD, 5.5mm x 550mm
CRADLE SLING ECONOMY
FDA UDI
DARCO INTERNATIONAL, INC.·00609271020771·Large
RIVA Posterior Fixation System
FDA UDI
XENIX MEDICAL LLC·00840493418520·CONSTRAINED STRAIGHT ROD, 6.0mm x 550mm
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 13, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORP.·Product code LZG·February 16, 2011
THERMACHOICE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code MKN·February 26, 2008
DISP.TROCAR THRD.W.DILATING PIN 12/110MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GCJ·July 9, 2019
Zimmer Hemovac Wound Drainage Device, Infection Control Kits, 400ml INF. CNTRL. Kit w/ 1/8" Drain Spec., 3,2mm, 10Fr, PVC, 107cm, medium, sterile, latex free, Rx only; Zimmer, Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio; REF 00-2550-702-10.
FDA Recall
Terminated
·Zimmer Inc.·Product code GCY·January 29, 2008