29 results
·
22ms
·
Sources: EU EUDAMED, US FDA
DEROYAL DRAPES, STERILE, NON-STERILE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N/A
FDA UDI
GEORGE TIEMANN & CO.·B5820303650·HOOK, SURGICAL, GENERAL & PLASTIC SURGERY
Osteoporotic Anchor 5.5mm (3 sutures)
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215164645·
ACCU-CHEK ADVANTAGE METER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
S.M.A.R.T NITINOL STENT ENDOSOPIC BILLARY SYSTEM (VARIOUS)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TriVerse Femoral Component CR
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215100148·
ACCUCHECK COMFORT CURVE
FDA Adverse Event
Malfunction
·ROCHE·Product code NBW·August 24, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 28, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS CORP.·Product code LFR·March 21, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 5, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 7, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 9, 2007
ICON 25 HCG (COMBO CASSETTE)
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code JHI·April 23, 2013
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS CORP.·Product code LFR·March 21, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS CORP.·Product code LFR·March 21, 2007
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CFR·October 19, 2006
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 23, 2007
ERBE
FDA Adverse Event
Malfunction
·LEONHARD LANG GMBH·Product code GEI·November 2, 2022
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS CORP.·Product code LFR·February 16, 2007
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·April 2, 2013