129 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·BioFreedom Drug Coated Coronary Stent System
SOL-M Syringe
FDA UDI
Sol-Millennium Medical, Inc.·00818392018240·SOL-M 20ml Luer Lock Syringe w/o Needle
OsteoMed
FDA UDI
OSTEOMED LLC·00845694052184·2.0mm x 0 Degree ExtremiFuse Implant
Greenwald Surgical Company, Inc.
FDA UDI
GRACE MANUFACTURING, INC.·10801334008086·Otis bougie-a-boule. stainless steel
LEONE SPA
FDA UDI
LEONE SPA·08033707069386·BIRD BEAK PLIERS ANGLE STYLE
Q-Rejuvalight Pro Facewear (Model: P19-0023)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
10.5MM X 10.7MM FLUTED DRUM SUPER LONG
FDA Adverse Event
Malfunction
·STRYKER IRELAND LTD.·Product code HBF·May 14, 2009
NA
FDA UDI
STRYKER CORPORATION·04546540373151·4.7mm x 7.9mm Fluted Drum
NA
FDA UDI
STRYKER CORPORATION·04546540373205·9.1mm x 7.9mm Fluted Drum
OsteoMed
FDA UDI
OSTEOMED LLC·00845694069922·ExtremiFuse 2mm 0 Degree Implant Sterile Qty 5
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·COBAS HPV TEST
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·COBAS 4800 BRAF V600 MUTATION TEST
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 8, 2008
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 7, 2013
UNICEL DXI 800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·August 4, 2011
COBAS 4800 HPV TEST, CE-IVD
FDA Adverse Event
ROCHE MOLECULAR SYSTEMS·Product code MAQ·December 22, 2011
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·cobas HPV Test
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·cobas HPV Test
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·cobas HPV Test
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·cobas® BRAF V600 Mutation Test