44 results · 25ms · Sources: EU EUDAMED, US FDA

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SpeediCath Compact Set

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

NA

FDA UDI
Synthes GmbH·10886982141576·1.5MM CORTEX SCREW SELF-TAPPING 20MM

OsteoMed

FDA UDI
OSTEOMED LLC·00845694057288·1.6mm Screw Block, ICON

Conventional Lead Apron .5mm Small 22 X 33

FDA UDI
Flow X Ray Corporation·00843696123062·Conventional Lead Apron .5mm Small, Royal Blue

Zavation

FDA UDI
Zavation LLC·00842166123298·Lateral Offset

MICROSCAN MICROSTEP PLUS PANEL NEW ANTIMICROBIAL - CEFUROXIME

FDA 510(k)
FDA Class 2 ·Microbiology

AVANAR F/X 2.9F INTRAVASCULAR ULTRASOUND IMAGING CATHETER, MODEL 85700

FDA 510(k)
FDA Class 2 ·Cardiovascular

Widex

FDA UDI
Widex A/S·05706069735581·Widex BEYOND B-F2 (Summer gold S-440 ) Telecoil...

GORE VIABAHN ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code NIP·December 4, 2012

GORE VIABAHN ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code NIP·December 4, 2012

BD GLIDE¿ WITH TBL BD ULTRA-FINE¿ NEEDLE INSULIN SYRINGE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·October 25, 2022

GORE VIABAHN ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES,INC·Product code NIP·December 4, 2012

GORE VIABAHN ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES,INC·Product code NIP·December 4, 2012

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 12, 2012

MBT CEM KEEL TIB TRAY SZ2.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code NJL·May 21, 2018

RESTORE ULTRA

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 24, 2014

LIGASURE V SEALER/DIVIDER

FDA Adverse Event
Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·March 31, 2011

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 2, 2013

QUICK SET PARADIGM

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·November 2, 2009

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 14, 2012