23 results
·
20ms
·
Sources: EU EUDAMED, US FDA
HM-CRYO
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FIXOS
FDA UDI
Stryker GmbH·07613252708797·Lid Screw-Rack 4.0mm
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981203399·Interbody, 9mm x 40mm x 14mm, 0 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981195403·Interbody, 9mm x 40mm x 14mm, 0 deg
SteriStretch® 3940-140
Device
EU MDR
·
Eu Md Class 1
·Eurotape B.V.·On the market·9 countries
OP-Stretch® 3940-140
Device
EU MDR
·
Eu Md Class 1
·Eurotape B.V.·On the market·9 countries
Arthrex®
FDA UDI
ARTHREX, INC.·00888867060364·ECLIPSE RESECT PROTECTOR,SZ S/40.0MM
IQ GUIDE WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
DOPPLER IMAGING OPTION
FDA 510(k)
FDA Class 2
·Radiology
UNKNOWN
FDA Adverse Event
WILLIAM COOK EUROPE·Product code DTK·October 27, 2015
ECLIPSE RESECT PROTECTOR,SZ M/46.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 29, 2024
ECLIPSE RESECT PROTECTOR,SZ L/50.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 23, 2024
ECLIPSE RESECT PROTECTOR,SZ M/46.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 23, 2024
ECLIPSE RESECT PROTECTOR,SZ S/40.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 3, 2024
AVL 6MM SUPERIOR DRILL, MODULAR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWE·May 23, 2024
3.0MM DRILL BIT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTW·June 7, 2024
ECLIPSE RESECT PROTECTOR,SZ S/40.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 1, 2024
ECLIPSE RESECT PROTECTOR,SZ S/40.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 1, 2024
ECLIPSE RESECT PROTECTOR,SZ S/40.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 1, 2024
ECLIPSE RESECT PROTECTOR,SZ S/40.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 1, 2024