19 results · 31ms · Sources: EU EUDAMED, US FDA

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THORA-CATH TROCAR-TYPE CHEST DRAINAGE TUBE

FDA 510(k)
FDA Class 2 ·General Hospital

NAR

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209117048·

Alcohol Well, 8.5mm

FDA UDI
KATALYST SURGICAL LLC·00840096207378·Alcohol Well, 8.5mm

InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S)

FDA 510(k)
FDA Class 2 ·Cardiovascular

EXPLOR MODULAR RADIAL HEAD REPLACEMENT DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 22, 2014

MICRO RECIPROCATING SAW

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·October 29, 2012

STARCLOSE SE VASCULAR CLOSURE SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code MGB·September 29, 2010

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·July 26, 2019

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021

VIDAS® ANALYZER

FDA Adverse Event
Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·June 3, 2021

2.7MM/3.5MM TI VA-LCP POSTLAT DHP/9H/LT/153MM-XLNG-STER

FDA Adverse Event
Injury ·SYNTHES RARON·Product code HRS·March 1, 2017

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·March 1, 2017