24 results
·
27ms
·
Sources: EU EUDAMED, US FDA
TERM GUARD 5000 UTERINE ACTIVITY
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
DD cubeY® HL
FDA UDI
Dental Direkt GmbH·EDDIG8430111·The DD cubeY® HL zirconium dioxide milling blan...
Silicone Urethral Catheter (Silicone Urethral Catheter)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
2014 InterActive/SwishActive System
FDA 510(k)
FDA Class 2
·Dental
VerSys®
FDA UDI
Zimmer, Inc.·00889024136427·
NA
FDA UDI
Zimmer, Inc.·00889024195059·
VerSys®
FDA UDI
Zimmer, Inc.·00889024136403·
VerSys®
FDA UDI
Zimmer, Inc.·00889024136410·
VerSys®
FDA UDI
Zimmer, Inc.·00889024136458·
NA
FDA UDI
Zimmer, Inc.·00889024195042·
VerSys®
FDA UDI
Zimmer, Inc.·00889024136434·
VerSys®
FDA UDI
Zimmer, Inc.·00889024136441·
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 2, 2014
RESTORE
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 21, 2012
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2015
FEMORAL HEAD +0X32MM DIA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·September 13, 2018
VerSys Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581
FDA Recall
Terminated
·Zimmer, Inc.·Product code LPH·May 19, 2014
REAGENT RED BLOOD CELLS IH-CELL A1 & B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·December 10, 2018
REAGENT RED BLOOD CELLS IH-CELL A1 & B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·December 10, 2018
REAGENT RED BLOOD CELLS IH-CELL A1 & B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·January 16, 2019