23 results · 29ms · Sources: EU EUDAMED, US FDA

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APTUS® Proximal Humerus System

FDA 510(k)
FDA Class 2 ·Orthopedic

LoFric® Elle™

FDA UDI
Wellspect AB·07333387024530·Single Use Urinary Catheter LoFric Elle Nelaton...

LoFric® Elle™

FDA UDI
Wellspect AB·07392532235429·Single Use Urinary Catheter LoFric Elle Nelaton...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X1814250·18mm x 14mm W x 25mm L x 0 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X18142580·18mm H x 14mm W x 25mm L x 8 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X181425120·18mm H x 14mm W x 25mm L x 12 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L181425120·18mm H x 14mm W x 25mm L XLIF Trial 12 degree L...

Origin 125º Short Neck Hip Stem

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215024079·

Best Medical International

FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365103926·

MICROSCAN DRIED GRAM-NEGATIVE MIC/COMBO PANEL, B1017 PANEL SERIES

FDA 510(k)
FDA Class 2 ·Microbiology

COOK VASCULAR INC. VITAL-PORT VASCULAR ACCESS SYSTEM POWER INJECTABLE PORT

FDA 510(k)
FDA Class 2 ·General Hospital

CART 9733856 S7 STAFF ASSEMBLED 110V

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LJT·November 4, 2015

STEALTHSTATION® S7´

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 20, 2019

CART 9733856 S7 STAFF ASSEMBLED 110V

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 17, 2019

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

*

FDA Adverse Event
Malfunction ·*·Product code FMF·June 17, 2013

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LJT·November 17, 2017

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 10, 2021