26 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE
FDA 510(k)
FDA Class 2
·Ophthalmic
DUPONT ALCOHOL CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Toxicology
POLYCATH-H CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
CC TIBIAL INSERT SZ 4, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 2, 2022
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·May 20, 2015
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·May 22, 2015
PREMICATH
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·April 20, 2015
PREMICATH
FDA Adverse Event
VYGON GMBH·Product code LJS·April 20, 2015
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·June 3, 2015
ASR ACETABULAR IMPLANT 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 11, 2013
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011
OT VERIO SYNC METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014
CC TIBIAL INSERT SZ 3, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 5, 2024
CC TIBIAL INSERT SZ 2, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 7, 2023
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 25, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 30, 2025
CC TIBIAL INSERT SZ 2, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 13, 2023
TRAPEZOID TIBIAL TRAY SZ 5F/5T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 25, 2024
23GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020
TRAPEZOID TIBIAL TRAY SZ 5F/5T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 30, 2025