28 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CHEMO-AIDE DISPENSING PIN
FDA 510(k)
FDA Class 2
·General Hospital
Implant Prosthetics
FDA UDI
Preat Corporation·00842092165317·Multi-Unit Verification Cylinder w/ .050 Screw
...
Implant Prosthetics
FDA UDI
Preat Corporation·00842092123508·Multi-Unit Verification Cylinder w/ .050 Screw ...
Alpha-Tec Systems
FDA UDI
Alpha-TEC Systems, Inc.·00816085024127·VTM Viral Transport Medium Pack
Implant Prosthetics
FDA UDI
Preat Corporation·00842092123584·Multi-Unit Verification Cylinder w/.050 Screw (...
QUASAR
FDA UDI
Modus Medical Devices Inc·G34350037300·MRgRT Insight - Indexing Accessory for Unity/MRSim
SCANLAN® Titanium Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159003574·DeBakey Micro Forceps, RH, 1 mm tips, 7-1/8"/18...
Implant Prosthetics
FDA UDI
Preat Corporation·00842092123515·Multi-Unit Verification Cylinder w/ .050 Screw ...
Implant Prosthetics
FDA UDI
Preat Corporation·00842092123607·Multi-Unit Verification Cylinder w/.050 Screw (...
IMPOAID
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GC FUJICEM
FDA 510(k)
FDA Class 2
·Dental
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC INC.·Product code KWP·October 15, 2009
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC INC.·Product code KWP·December 31, 2009
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·February 12, 2013
RESTORE ULTRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 24, 2011
LIGASURE LAPAROSCOPIC SLR/DIV
FDA Adverse Event
Malfunction
·COVIDIEN LP (US SURGICAL)·Product code GEI·February 20, 2008