9 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACCENT DG(TM) BALLOON ANGIOPLASTY CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Lower ROC Pack for Herbst LL5 10mm
FDA UDI
SPECIALTY APPLIANCES, LLC·D8199006770·
INNOPORT LAPAROSCOPIC ACCESS DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ZUMA GUIDE CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
SMR FINNED HUMERAL BODY
FDA Adverse Event
Malfunction
·LIMACORPORATE SPA·Product code HSD·July 18, 2019
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·June 27, 2014
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 8, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 16, 2010
ZUMA Z2 7F GUIDE CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC, INC·Product code DQY·June 12, 2020