21 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Imbio Segmentation Editing Tool software
FDA 510(k)
FDA Class 2
·Radiology
Super Upper Limbs Versalock Plating System
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663678·VERSALOCK ULNA/RADIUS HOOK PLATE 49.0mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012146·PedFuse Respond, SLD, 8.0mm x 70mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012153·PedFuse Respond, SLD, 8.0mm x 75mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012092·PedFuse Respond, SLD, 8.0mm x 45mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012122·PedFuse Respond, SLD, 8.0mm x 60mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012160·PedFuse Respond, SLD, 8.0mm x 80mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012061·PedFuse Respond, SLD, 8.0mm x 30mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012139·PedFuse Respond, SLD, 8.0mm x 65mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012108·PedFuse Respond, SLD, 8.0mm x 50mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012078·PedFuse Respond, SLD, 8.0mm x 35mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012115·PedFuse Respond, SLD, 8.0mm x 55mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012085·PedFuse Respond, SLD, 8.0mm x 40mm
AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO X
FDA 510(k)
FDA Class 2
·Cardiovascular
SECURE IMPLANT SYSTEM (2.5/3.0MM)
FDA 510(k)
FDA Class 2
·Dental
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 24, 2016
LIGAMAX-5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 27, 2011
KEEPSAFE FALL MONITOR
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·June 4, 2013
EVIS EXERA II BRONCHOVIDEOSCOPE
FDA Adverse Event
Injury
·OLYMPUS MED SYSTEMS CORP·Product code EOQ·October 15, 2014
VERSAFITCUP ACETABULAR SHELL CC Ø 56
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MEH·August 12, 2019