9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TIP & MEMBRANE ASSEMBLY
FDA 510(k)
FDA Class 2
·Ophthalmic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123809·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 100mm
Mediflex Modular III Basic Laparoscopic Instruments
FDA UDI
FLEXBAR MACHINE CORPORATION·00842102104138·Modular 3 Adhesion Grasper,Ratcheted Handle/Sha...
56 SERIES JET NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
JOURNEY II CR KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
UNK
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC.·Product code KNS·June 13, 2014
NEXGEN LPS-FLEX GSF FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·January 9, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 6, 2014