8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
INFANT FLOW NCPAP MASKS
FDA 510(k)
FDA Class 2
·Anesthesiology
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984254·anteriors; shade B1; mould R 89
CIRCON ACMI BICAP III THERAPEUTIC SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HYPAFIX DRESSING RETENTION SHEET
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 10, 2011
ADULT ROTATING CRANIOTOME
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013
InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.
FDA Recall
Terminated
·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009