22 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ESTECH AORTIC EASY FLOW CANNULA
FDA 510(k)
FDA Class 2
·Cardiovascular
Nova
FDA UDI
PURELIFE, LLC·D79010601011·Nova Nitrile Powder-Free, X-Small, Super-stretc...
“Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)
FDA UDI
Paonan Biotech Co.,Ltd.·04719878788984·Cannulated T-Handle
Medallion®
FDA UDI
Merit Medical Systems, Inc.·00884450006603·
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0600010·Tray Insert, Level 1
Ocata Anterior Cervical System
FDA UDI
Kalitec Direct LLC·B07308K0600010·Tray Insert 1, Ocata
RX VIATRAC 14 PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SUPPORT ARM 176
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code IOY·February 11, 2015
SPACEOAR VUE SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OVB·October 29, 2024
ENDOTAK RELIANCE G
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LWS·December 3, 2024
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 20, 2013
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·April 15, 2011
8010042-2008-00054
FDA Adverse Event
Malfunction
·Product code ---·May 2, 2008
LGC TIBIAL FIT TRAY CEM SZ 3.5F / 3.5T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 22, 2024
PULSE GEN MODEL UNK
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code LYJ·March 8, 2024
AMPLATZ SUPER STIFF
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code EZB·June 5, 2025
INOGEN EL ICD DR
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LWS·February 11, 2025
FARAWAVE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code QZI·March 13, 2025
IMPLANTABLE DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LWP·March 17, 2026