9 results
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18ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HUMAN REFERENCE SERUM C4 COMPLEMENT
FDA 510(k)
FDA Class 2
·Immunology
Avance
FDA UDI
Mölnlycke Health Care AB·07323190166442·
Symmetry Surgical
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482125830·Symmetry® Rasp, Nail, Angled, Double-Ended, Ser...
HAND REAMERS
FDA 510(k)
FDA Class 1
·Orthopedic
LIEBERMAN POLACK DOUBLE CORNEAL FORCEPS
FDA 510(k)
FDA Class 1
·Ophthalmic
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 2, 2012
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 2, 2014
ACCU-CHEK COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·September 18, 2007
STANDALONE PMP NEONATAL OXYGENATOR
FDA Adverse Event
Malfunction
·EUROSETS S.R.L.·Product code QNR·August 2, 2024