7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOPAK MEASUREMENT SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981563·anteriors; shade A2 light; mould UM2
TRYPTOSE PHOSPHATE BROTH
FDA 510(k)
FDA Class 1
·Microbiology
The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C with BioGUARD Technology
FDA 510(k)
FDA Class 2
·Cardiovascular
INFUSOR
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 27, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 31, 2011
SOFTCLIX ® PLUS GT LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·August 5, 2014