7 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INERTIA® CONNEXX Modular Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881
FDA 510(k)
FDA Class 2
·General Hospital
QUICKNIT
FDA 510(k)
FDA Unclassified
·Unknown
GENEPATH
FDA Adverse Event
Other
·BIO REFERENCE LAB·Product code MVU·October 31, 2014
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·July 15, 2013
Revogene, Catalog no. 610210. IVD test instrument
FDA Enforcement
Class II
·Ongoing·Meridian Bioscience Inc·August 3, 2022