11 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SYVA EDMS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909120552·REVELATION DIAMOND 805-016M - 5 PACK
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668110843·TIP GUARDS VENTED ASSORTED PACK OF 100
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668110898·TIP GUARDS VENTED YELLOW PACK OF 100
AMSCO CHIMERON MEDIUM STEAM STERILIZER
FDA 510(k)
FDA Class 2
·General Hospital
3.25MM SPLINE TWIST IMPLANT
FDA 510(k)
FDA Class 2
·Dental
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 12, 2021
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 4, 2017
REPLACEMENT POWER BRUSH HEAD
FDA Adverse Event
Malfunction
·RANIR, LLC·Product code JEQ·May 13, 2014
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 1, 2010
TOTAL ASR FEM IMP SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·January 11, 2013