15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AIR PURGE CONTROL SYSTEM FOR S5 SYSTEM MODEL 23-45-05
FDA 510(k)
FDA Class 2
·Cardiovascular
LEONE SPA
FDA UDI
LEONE SPA·08033707065722·INTRAORAL ELASTICS 4,5 oz 3/8" orange
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122162·KWire .035x4" (0.9x100mm)
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450215692·
Orthopedic Instruments
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258660738·
ULTRA PRESERVE WITH ALOE VERA (GREEN) NATURAL RUBBER LATEX EXAMINATION GLOVE MADE FROM ALLOTEX AN ENZYME TREATED NATURAL
FDA 510(k)
FDA Class 1
·General Hospital
TENODESIS SCREW, 5.5 MM, MODEL AR-1350-55
FDA 510(k)
FDA Class 2
·Orthopedic
ROD, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019
PRONTO SPOT CHECK PULSE CO-OXIMETER
FDA Adverse Event
Malfunction
·MASIMO - 40 PARKER·Product code DQA·July 9, 2018
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013
EBI OSTEOGEN IMPLANTABLE GROWTH STIMULATOR
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code LOE·August 5, 2008
3002 MASTER BOMS
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 11, 2011
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·September 29, 2015
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·September 29, 2015
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·September 29, 2015