32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MT ALERT INFUSION MONITOR
FDA 510(k)
FDA Class 2
·General Hospital
Tandem Mobi Autosoft 30 Kit
FDA UDI
Tandem Diabetes Care, Inc.·00389152312170·Autosoft 30, 23"/13mm, 10 pack kit
TAG
FDA UDI
Smith & Nephew, Inc.·03596010024657·TAG 3.7MM WEDGE (BX 1) STERILE
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0132110·Trial, TLIF, 27L OB CRV 7Deg, 11mm
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033465134·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033465127·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033465110·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033465103·
MYSONO 201 DIAGNOSTIC ULTRASOUND AND TRANSDUCERS
FDA 510(k)
FDA Class 2
·Radiology
STERILE BUTTON PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001312110010·Retention Plate, Oblique-Only, Small, 10 mm
E-Guard Blue
FDA UDI
Envisiontec GmbH·04260683220041·E-Guard Blue is a light-curing material for the...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001312111180·Retention Plate, Oblique-Only, Small, 11 mm - 1...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001312112180·Retention Plate, Oblique-Only, Small, 12 mm - 1...
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 21, 2020
XPS® BUR GUARD - VISAO®
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ERL·April 22, 2016
SMR SHOULDER
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code KWT·May 27, 2026
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 20, 2013
INRATIO
FDA Adverse Event
ALERE SAN DIEGO, INC·Product code GJS·March 1, 2011
BOOMERANG CATALYST SYSTEM
FDA Adverse Event
Injury
·CARDIVA MEDICAL, INC.·Product code MGB·March 14, 2008