23 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Grandio blocs
FDA 510(k)
FDA Class 2
·Dental
NA
FDA UDI
KEY SURGICAL, INC.·10849771049309·K-Wires, Double diamond, .028-inch (0.7mm) diam...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292923·
K-Wire w. double end lanzet point 0.71mm/102mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM712000·K-Wire w. double end lanzet point
0.71mm...
AOS HUMERAL NAIL 7.0mm x 20cm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016833·
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484474·K-Wire w. double end lanzet point _x000D_...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690189947·Tibial Tray Drill
3.5mm x 200mm Cervical Rods
FDA UDI
XENCO MEDICAL LLC·B064XM21712002·
Ø3.5mm X 110mm PRECONTOURED CERVICAL RODS
FDA UDI
XENCO MEDICAL LLC·B064XMPH21712002·
PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MAC-LAB SYSTEM, CARDIOLAB SYSTEM, COMBOLAB SYSTEM, SPECIALSLAB SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
JOSTENT GRAFTMASTER
FDA Adverse Event
Death
·AV-TEMECULA-CT·Product code MAF·June 14, 2013
UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JGS·July 1, 2011
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE SYSTEM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NTE·September 22, 2008
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE GMBH·Product code NBW·April 27, 2020
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE GMBH·Product code NBW·April 27, 2020
3.0MM TI-SCREWANCHOR1BLUE SUTU
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·May 4, 2018
3.0MM TI-SCREWANCHOR1BLUE SUTU
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·March 15, 2018
3.0MM TI-SCREWANCHOR1BLUE SUTU
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·March 12, 2018
3.0MM TI-SCREWANCHOR1BLUE SUTU
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·May 4, 2018