17 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRI-POLAR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
STERILMED, INC.·10888551007542·SAW BLADE SAGITTAL K9 K2000 SERIES
11G BLADED MAMMOTOME ST PROBE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006
TECHNICON HDL CHOLESTEROL METHOD
FDA 510(k)
FDA Class 1
·Clinical Chemistry
OSW Aligner System
FDA 510(k)
FDA Class 2
·Dental
MAMMOTOME CONTROL MODULES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006
MAMMOTOME CONTROL MODULES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006
MAMMOTOME HARDWARE HOLSTER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006
MAMMOTOME CONTROL MODULES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006
MAMMOTOME CONTROL MODULES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006
STERRAD 100S STERILIZER
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 8, 2006
MAMMOTOME CONTROL MODULES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006
MAMMOTOME CONTROL MODULES
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code KNW·June 13, 2006
ALTRX +4 NEUT 36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 7, 2013
INRATIO
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC.·Product code GJS·February 7, 2011
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
STERRAD 100NX STERILIZER 1-DR
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 6, 2021