34 results · 21ms · Sources: EU EUDAMED, US FDA

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RESONANCE METALLIC URETERAL STENT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·December 13, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 31, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 6, 2023

RESONANCE STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FAD·July 25, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·May 29, 2015

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 11, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·November 22, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·September 27, 2023

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·August 13, 2018

RESONANCE STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FAD·September 12, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·August 16, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·January 22, 2019

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496063742·SOCKS FOR YOU FREEDOM EASY, SIZE L, BORDEAUX, A...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137169·Ti-6Al-4V ALIF Implant 42 X 32, 19mm Height 28°...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137152·Ti-6Al-4V ALIF Implant 42 X 32, 17mm Height 28°...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137176·Ti-6Al-4V ALIF Implant 42 X 32, 21mm Height 28°...

SCULPTURE PLUS NANO-HYBRID COMPOSITE

FDA 510(k)
FDA Class 2 ·Dental

BOSTON SCIENTIFIC V-18 CONTROL WIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

GII ARTICULAR INSERTER/EXTRACT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018