18 results
·
23ms
·
Sources: EU EUDAMED, US FDA
ABBOTT CMV TOTAL ANTIBODY EIA (MODIFICATION)
FDA 510(k)
FDA Class 2
·Microbiology
3M™ Victory Series™
FDA UDI
3M UNITEK CORPORATION·00652221117366·3M™ Victory Series™ First Molar Bands Kit 954-3...
PLEUR-EVAC II AUTOTRANSFUSION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
DU PONT DIMENSION(R) SALICYLATE(SAL) METHOD
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BD ANGIOCATH¿ IV CATHETER 22 G X 1"
FDA Adverse Event
Malfunction
·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·May 20, 2015
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·May 22, 2015
PREMICATH
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·April 20, 2015
PREMICATH
FDA Adverse Event
VYGON GMBH·Product code LJS·April 20, 2015
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·June 3, 2015
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·January 9, 2013
ASR UNI FEMORAL IMPL SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 5, 2011
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014
BD ANGIOCATH¿ IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017
23GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020
25GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026
Alcon Custom Pak
FDA Enforcement
Class II
·Ongoing·Alcon Research, LTD.·August 23, 2023