29 results · 22ms · Sources: EU EUDAMED, US FDA

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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