12 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)
FDA 510(k)
FDA Class 2
·Dental
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171028369·PESSARY, GEHRUNG #8, 90mm
CANADY PLASMA ELECTROSURGICAL UNIT SERIES WITH ACCESSORY PROBES AND BLADES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
JEIL BONE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
TAMPAX RADIANT TAMPON UNSCENTED, ABSORBENCY UNKNOWN
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·March 10, 2021
TAMPAX RADIANT TAMPON UNSCENTED, ABSORBENCY UNKNOWN
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·March 3, 2021
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 6, 2013
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 22, 2011
Phoenix AP AST Indicator Bag, Catalog Number 246006
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·March 6, 2019
BD¿ ORAL DISPENSING SYRINGE 1 ML
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code KYW·May 12, 2020
Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020
FDA Enforcement
Class II
·Terminated·Cardinal Health 200, LLC·February 26, 2020