17 results · 21ms · Sources: EU EUDAMED, 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