10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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8 X 10 NON-STICK PAD
FDA 510(k)
FDA Unclassified
·Unknown
3M™ ESPE™
FDA UDI
3M COMPANY·30605861030893·3M™ ESPE™ Gold Anodized Crown Refills, First Mo...
VARIAX
FDA UDI
Stryker GmbH·07613327123548·Labeling Clip Wrist Add-on Drawer 1
N/A
FDA UDI
Tyber Medical, LLC·M695M9403440·
PDI PREPMASTER WET PACK MINOR PROCEDURE
FDA 510(k)
FDA Class 2
·General Hospital
IMPAX OT3000 ORTHOPEDIC WORKSTATION
FDA 510(k)
FDA Class 2
·Radiology
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·June 26, 2014
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIV·Product code FNL·December 9, 2010
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·February 2, 2013
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
FDA Enforcement
Class II
·Terminated·Capintec Inc·April 1, 2020