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

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FRESENIUS MEDICAL TREATMENT CHAIR T688 SERIES

FDA 510(k)
FDA Class 2 ·Physical Medicine

n/a

FDA UDI
HANS RUDOLPH, INC.·00874750007097·3700B PNT/HTRSHELL/CONN ASSY

UniTip Catheter

FDA UDI
Unisensor AG·07640172971390·

CORELEADER HEMO-PAD MODEL CPII 02030

FDA 510(k)
FDA Unclassified ·Unknown

POWER DRIVE

FDA 510(k)
FDA Class 1 ·Dental

LGN PS HIGH FLEX XLPE SZ 1-2 13MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

CRE¿ WIREGUIDED

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·February 20, 2013

CRE¿ WIREGUIDED

FDA Adverse Event
Death ·BOSTON SCIENTIFIC - CORK·Product code KNQ·September 7, 2012

CRE? WIREGUIDED

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·June 18, 2013

LGN PS HIGH FLEX XLPE SZ 1-2 13MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

CRE¿ WIREGUIDED

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·January 7, 2013

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 14, 2013

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 25, 2011

CRE¿ WIREGUIDED

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·March 13, 2013

CRE¿ WIREGUIDED

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·August 10, 2012

CRE? WIREGUIDED

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·June 6, 2013

CRE¿ WIREGUIDED

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code KNQ·December 5, 2012

CRE¿ WIREGUIDED

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code KNQ·July 2, 2012

smiths medical portex, Nasopharyngeal Airway, Sizes as follows: a) AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060; b) AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060JP; c) AIRWAY NASOPHARYNGEAL 7.0MM, REF 100/210/070; d) AIRWAY NASOPHARYNGEAL 7.0MM, REF 100/210/070JP; e) AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080; f) AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080JP; g) AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080JS; h) AIRWAY NASOPHARYNGEAL 9.0MM, REF 100/210/090; i) AIRWAY NASOPHARYNGEAL 9.0MM, REF 100/210/090JP;

FDA Enforcement
Class II ·Ongoing·Smiths Medical ASD Inc.·October 30, 2024