20 results
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20ms
·
Sources: EU EUDAMED, US FDA
MAXI-FLOW
FDA 510(k)
FDA Class 2
·General Hospital
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192039·Apex Revision Knee Reamer - Zimmer 15mm
3M™ Victory Series™
FDA UDI
3M UNITEK CORPORATION·00652221117786·3M™ Victory Series™ Second Molar Bands, 955-150...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938627·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937453·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939792·Percutaneous Transluminal Angioplasty Balloon C...
REMOVE ADHESIVE REMOVER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS
FDA 510(k)
FDA Unclassified
·Unknown
PATHROMTIN SL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017
PATHROMTIN SL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017
STOCKERT S3 LEVEL SENSOR MOUNTING PADS
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTW·August 2, 2012
SENSOR MODULE LEVEL/BUBBLE
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTW·May 11, 2012
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 11, 2013
RIATA ST ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·July 10, 2014
STOCKERT S3 LEVEL SENSOR MOUNTING PADS
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DWA·January 6, 2012
PATHROMTIN SL (RILIBAK)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·January 4, 2023
S5 BUBBLE DETECTOR SENSOR 3/16''
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code KRL·February 25, 2022
STOCKERT S3 LEVEL SENSOR MOUNTING PADS
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTW·January 6, 2012
REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 22/200
FDA Adverse Event
Injury
·ZIMMERSWITZERLAND MANUFACTURING GMBH·Product code KWA·July 27, 2020