7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
FDA 510(k)
FDA Class 1
·Radiology
Bun-Yo-Matic™ Lapidus Clamp System
FDA UDI
Paragon 28, Inc.·00889795131324·Bun-Yo-Matic, K-wire, Ø2.30mm x 19cm, Smooth
CALIBRATOR FOR AUTOMATED SYSTEMS (C.F.A.S.), MODEL 10759350 360
FDA 510(k)
FDA Class 2
·Clinical Chemistry
BabyDance Fertility Lubricant
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PROLENE POLYPROPYLENE MESH
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·February 14, 2013
ASR ACETABULAR IMP 54
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·January 7, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014