9 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COUNTER, DISPOSABLE SURGICAL NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
Hillrom™
FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761990371·Trumpf Medical/Medizin Shoulder basis segment S
ReLine
FDA UDI
Nuvasive, Inc.·00887517005960·RELINE-C Bender Tip, Ø3.5 Str Coronal
VALVE, I.M.V. (U-MID ONE WAY)
FDA 510(k)
FDA Class 2
·Anesthesiology
EchoSure Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·May 13, 2024
PULSE GEN MODEL 103
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·May 5, 2014
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 15, 2012
POLY-L-LACTIC ACID (POLY-L-LACTIC ACID)
FDA Adverse Event
Injury
·SANOFIAVENTIS U.S. LLC·Product code LMH·August 3, 2010