25 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Neodent Implant System - Temporary Abutments
FDA 510(k)
FDA Class 2
·Dental
MultiPulse HoPLUS
FDA UDI
Asclepion Laser Technologies GmbH·04058784001986·Holmium Laser for Surgery
Obturator
FDA UDI
SOPRO-COMEG GmbH·04059082032887·
Trocar
FDA UDI
SOPRO-COMEG GmbH·04059082005898·
Trocar
FDA UDI
SOPRO-COMEG GmbH·04059082032849·
Obturator
FDA UDI
SOPRO-COMEG GmbH·04059082005904·
Trocar
FDA UDI
SOPRO-COMEG GmbH·04059082005867·
Trocar
FDA UDI
SOPRO-COMEG GmbH·04059082032870·
Arthroscopy sheath
FDA UDI
SOPRO-COMEG GmbH·04059082005850·
Arthroscopy sheath
FDA UDI
SOPRO-COMEG GmbH·04059082032863·
Obturator
FDA UDI
SOPRO-COMEG GmbH·04059082032856·
Arthroscopy sheath
FDA UDI
SOPRO-COMEG GmbH·04059082005881·
Arthroscopy sheath
FDA UDI
SOPRO-COMEG GmbH·04059082032832·
Obturator
FDA UDI
SOPRO-COMEG GmbH·04059082005874·
NAVIAID ICVI DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GAS TRANSFILL
FDA 510(k)
FDA Class 2
·Anesthesiology
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 30, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 14, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 19, 2011
HARMONIC ACE 36 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 9, 2008