50 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Electronic Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
OPERATING SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055520·OPERATING SCISSORS STRAIGHT SHARP BLADES POWER ...
RETRACTOR CHEEK/LIP, 10 x 40MM TOE UP
FDA UDI
W.H. Holden, Inc.·D9282007160·
RETRACTOR CHEEK/LIP, 10 x 55MM TOE UP
FDA UDI
W.H. Holden, Inc.·D92820071610·
RETRACTOR CHEEK/LIP, 10 x 65MM TOE UP
FDA UDI
W.H. Holden, Inc.·D9282007161SPEC0·
RETRACTOR CHEEK/LIP, 10 x 80MM TOE UP
FDA UDI
W.H. Holden, Inc.·D92820071620·
Orbitum Staple System
FDA UDI
CPM Medical Consultants, LLC·B565FO2007161·Punch VI 16mm
RAPID OPIATES TEST STRIP II, RAPID OPIATES TEST CARD II AND DOA MULTIPLE DRUG TEST CARDS (UP TO SIX TESTS)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ACCESS CK-MB ON THE ACCESS IMMUNOASSAY ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CADD CASSETTE 100ML W/FLOWSTOP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code LHI·March 2, 2022
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·February 29, 2008
PULSE GEM MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·February 29, 2008
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·February 29, 2008
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
GORE PRECLUDE DURA SUBSTITUTE
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code GXQ·June 25, 2013
GORE PRECLUDE DURA SUBSTITUTE
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code GXQ·June 25, 2013
GORE PRECLUDE DURA SUBSTITUTE
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code GXQ·June 26, 2013
GORE PRECLUDE DURA SUBSTITUTE
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code GXQ·June 26, 2013
GORE PRECLUDE DURA SUBSTITUTE
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code GXQ·June 25, 2013
DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM DEXCOM SHARE SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·October 29, 2015