9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ELIPAR TRILIGHT
FDA 510(k)
FDA Class 2
·Dental
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984247·anteriors; shade B1; mould D 82
DPC T60I KUSTI, MODEL 984248; DPC T60I, MODEL 984247
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MODIFIED DDI SEROCARD RUBELLA IGG TEST KIT
FDA 510(k)
FDA Class 2
·Microbiology
PERIODONTAL IRRIGATING SOLUTION-D
FDA 510(k)
FDA Class 2
·Dental
SUPRACONDYLAR NAIL T2 SCN 10 X 200 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS ¿ KIEL·Product code HSB·July 17, 2012
RIATA ST ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013
PUMP,COLLEAGUE SINGLE CHANNELCOLOUR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 10, 2011
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·August 6, 2014