8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K
FDA 510(k)
FDA Class 2
·Neurology
artegral
FDA UDI
Merz Dental GmbH·D7091970639·anteriors; shade A3.5 light; mould CM
NON-STERILE, POWDER-FREE NITRILE EXAMINATION GLOVE, BLUE WITH POLYMER COATING
FDA 510(k)
FDA Class 1
·General Hospital
HEALIX ADVANCE Anchor with PERMATAPE Suture
FDA 510(k)
FDA Class 2
·Orthopedic
ROOT CANAL INSTRUMENT
FDA Adverse Event
Other
·MICRO-MEGA SA·Product code EKS·January 25, 2010
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 2, 2014
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 20, 2013
ACCU-CHEK ® COMPACT PLUS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·January 25, 2011