37 results · 20ms · Sources: EU EUDAMED, US FDA

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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