17 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·DACRON SURGICAL SUTURES
DESS dental smart solutions
FDA UDI
TERRATS MEDICAL SL.·08435457209959·Internal Hex "Click"
VAN-TEC ENDOPYELOTOMY KNIFE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code HQL·June 23, 2006
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·N-18 (KOLFOCON A),N-32 (KOLFOCON B) LENS MATERIAL
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·EPCON SOFT (POLYMACON) SPHERICAL AND TORIC LENSES
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·N-18 (KOLFOCON A),N-32 (KOLFOCON B) LENS MATERIAL
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·EPCON SOFT (POLYMACON) SPHERICAL AND TORIC LENSES
SILICONE ULTRAVIOLET ABSORBING POSTERIOR CHAMBER SINGLE PIEC
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code HQL·June 15, 2006
SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code HQL·June 8, 2006
*
FDA Adverse Event
Malfunction
·STAAR SURGICAL·Product code HQL·June 15, 2006
SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·June 26, 2006
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 22, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 31, 2014
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·December 19, 2012
SEE H-10
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code HQL·October 10, 2012
SEE H-10
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code HQL·March 27, 2012