42 results
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32ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SUCTION IRRIGATION ELECTRODES AND ADAPTERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094070729·Welch Allyn PCH-100 Holter Office Software Kit ...
Ormco
FDA UDI
ORMCO CORPORATION·00889989027259·SS BROAD ARCH UP LGE 0160X0220 PK/10
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869691840·MOSS Pedicle Screw Inserter ISR20 ; cannulated ...
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361005650·Arena-L, 35x26, Lordotic 12 degrees, 11H
VersaTrode™
FDA UDI
GRAPHIC CONTROLS ACQUISITION CORP·10813150021040·
VersaTrode™
FDA UDI
GRAPHIC CONTROLS ACQUISITION CORP·30813150021044·
ECOTRACT ADJUSTABLE WOUND PROTECTOR/RETRACTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FISHER & PAYKEL HEALTHCARE BUBBLE CPAP SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
NEONATAL BUBBLE CPAP DUAL HEATED CIRCUIT KIT
FDA Adverse Event
Malfunction
·Product code BZE·March 3, 2021
NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code HRS·April 4, 2023
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 8, 2013
ESTEEM SYNERGY 2 PC - 2PC STOMAHESIVE (SH) WAFER W/FLEXIBLE COLLAR
FDA Adverse Event
Injury
·CONVATEC, INC.·Product code EXE·September 12, 2014
ENDURANT STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·May 18, 2011
BUBBLE CPAP CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·April 19, 2011
BUBBLE CPAP CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·April 19, 2011
BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer¿ Push Button Blood Collection Set with the needle protector removed prior to needle retraction.
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Company·October 30, 2019
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FMI·June 26, 2019
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·June 26, 2019
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·June 11, 2019