10 results
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18ms
·
Sources: EU EUDAMED, US FDA
R2 PADDLE TYPE CABLE-ADAPTOR #S 170,171
FDA 510(k)
FDA Class 2
·Cardiovascular
Polishers
FDA UDI
DFS - DIAMON GmbH·04057176147714·UPORAL C wheel CA, PU: 6 pcs
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209112913·
CONFORMIS TOTAL KNEE REPIAR SYSTEM (ITOTAL) TIBIAL COMPONENT: 6.0 MM THICKNESS
FDA 510(k)
FDA Class 2
·Orthopedic
VAPR 2.3MM WEDGE ELECTRODE FOR USE WITH VAPR SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GYNECARE TVT-ABBREVO MINI LCM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·November 30, 2021
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·May 8, 2014
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·October 18, 2012
CENTRAL LINE
FDA Adverse Event
Injury
·ARROW·Product code DQO·August 10, 2010
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021