37 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OXY-1 System
FDA 510(k)
FDA Class 2
·Cardiovascular
Zirlux
FDA UDI
HENRY SCHEIN, INC.·00304040188101·ZIRLUX ML DISC C4 98x25
D-10
FDA UDI
BIO-RAD LABORATORIES, INC.·00847817003271·D-10 Hemoglobin A1c Supplemental Reagent Pack
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776165352·ROU RETRACTOR LARGE . LONG
Guide Sleeve
FDA UDI
Treace Medical Concepts, Inc.·00810111221696·Guide Sleeve
DEBAKEY TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896059955·DEBAKEY TISSUE FORCEPS FLAT HANDLE
Bradshaw Medical Inc.
FDA UDI
Bradshaw Medical, Inc.·00810019930102·BIT, HEX MALE 5/64" AO
ELMED
FDA UDI
ELMED INCORPORATED·00842180175594·HULKA UTERINE MANIPULATOR TENACULUM
SIGMA DIAGNOSTICS ACCUCLOT LA CONTROL
FDA 510(k)
FDA Class 2
·Hematology
LOGIFLEX LAPAROSCOPIC BAND POSITIONING DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SURELIFE ARM BP MONITOR-PREMIUM
FDA Adverse Event
Malfunction
·MHC MEDICAL PRODUCTS, LLC·Product code DXN·June 19, 2018
BLUNT TIP SCREW, ÿ 4X38MM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSB·October 24, 2024
DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER
FDA Adverse Event
Injury
·MPRI·Product code LWS·April 13, 2013
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·Product code BTT·July 29, 2020
PROLIEVE THERMODILITATION KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 15, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 1, 2013
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 29, 2016
BLUNT TIP SCREW, ÿ 4X38MM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSB·October 24, 2024
PROXIMAL HUMERUS, LEFT, ÿ 7X160MM
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code HSB·October 8, 2024