15 results
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40ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GLUCOCARD 01-MINI BLOOD GLUCOSE MONITORING SYSTEM, RELION MICRO BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SENTRI™ INTERSURGICAL ECOLITE™, ADULT, MASK WITH CO MONITORING LINE AND TUBE
FDA UDI
Intersurgical Incorporated·05030267169634·SENTRI™ INTERSURGICAL ECOLITE™, ADULT, MASK WIT...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694043809·2.0mm 4 Hole Straight Locking Plate, 2.0mm thick
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741420350·
LEONE SPA
FDA UDI
LEONE SPA·08033707011194·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 35
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L142035120·14mm H x 20mm W x 35mm L XLIF Trial 12 degree L...
BD NEEDLE ECLIPSE 25X1 RB BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·September 22, 2024
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674142035060·
SLEEK OTW PTA CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
ALUMINA HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·June 3, 2013
AU2700 CLINICAL CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER MISHIMAK.K.·Product code JGS·June 28, 2011
SLEEK OTW PTA CATHETER
FDA Adverse Event
Injury
·CLEARSTREAM TECHNOLOGIES LTD.·Product code DQY·December 13, 2023
Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016, 135028, 135029, 936400, 936400BLU. Microlab AT+ and Microlab AT+2, part numbers 142000, 142001, 142001R, 142002, 142003, 142005, 142006, 142006R, 142007, 142008, 142009, 142015, 142017, 142035, 142036
FDA Recall
Terminated
·Hamilton Co·Product code JTC·December 13, 2005