47 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SURVEYOR S4 MOBILE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E89611410200·Grasping forceps Russian model
ELMED
FDA UDI
ELMED INCORPORATED·00842180170261·Single Ended Hegar Dilator, 20mm Tip, Autoclava...
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515234598·Cushing Bayonet Bipolar Fcps, insltd, 1.5mm tip...
PAQ.245X300X1000/EEG/141020
FDA UDI
AB MEDICA GROUP, S.A.·08428763006916·
PAQ.245X300X0500/EEG/141020
FDA UDI
AB MEDICA GROUP, S.A.·08428763007029·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311410200·
Life Instruments
FDA UDI
Life Instrument Corporation·M93071410201U0·Micro Axial Curette #2/0 ANG UP
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16720031410200·
Life Instruments
FDA UDI
Life Instrument Corporation·M93071410200U0·Micro Axial Curette #2/0 STR UP
ATRICURE DISSECTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CADSTREAM VERSION 3.1
FDA 510(k)
FDA Class 2
·Radiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 13, 2024
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 5, 2025
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·October 3, 2014
BONE SCREW, CROSS-PIN, SELF-TAPPING, DIAM.1.2X6MM, UPPERFACE, STERILE, (1/PACKAG
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code JEY·June 3, 2013
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·June 16, 2011
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018