28 results
·
23ms
·
Sources: EU EUDAMED, US FDA
GENERIC BLOOD GLUCOSE TEST STRIP
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040062418·Endoflex Reamers 25 mm
CUSTOM PROCEDURE KIT
FDA UDI
MEDIVATORS INC.·40677964009868·The ENDO CARRY-ON Procedure Kit contains all of...
Implant Prosthetics
FDA UDI
Preat Corporation·00842092102213·Branemark®-compatible RP 30° Multi-Unit Abutmen...
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693214636·Cassettes are designed to contain incised tissu...
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001092·artVeneer life lower anteriors, UBS, A3
CD61 APC
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Shenzhen Wellgrow Biotech Co., Ltd.·1 device
E3 MICROPROB SERIES OF LASERS AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
WAKO LIPASE CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SYNCARDIA FREEDOM ONBOARD BATTERY
FDA Adverse Event
Malfunction
·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 19, 2022
SYNCARDIA FREEDOM ONBOARD BATTERY
FDA Adverse Event
Malfunction
·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 21, 2022
STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·May 23, 2019
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 24, 2011
NOVASURE IMPEDANCE CONTROLLED EA SYSTEM
FDA Adverse Event
Injury
·CYTYC SURGICAL PRODUCTS·Product code MNB·February 22, 2008
RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·May 23, 2019
RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·May 23, 2019
RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·May 23, 2019
COBALT HV BONE CEMENT 40G
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LOD·February 9, 2012
SYRINGE BOIN TUBE 10ML 21G 1-1/4IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·October 13, 2020