9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
PUMP, BALLOON, INTRA-AORTIC, TRI-SEGMENT
FDA 510(k)
FDA Class 2
·Cardiovascular
ALIF
FDA UDI
Nuvasive, Inc.·00887517640284·ALIF Interfixated Guide, Single L
The Orthodontic Store
FDA UDI
Young Innovations, Inc.·00843471185186·.022 U/R Std. Comb. Weld Sz#21
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515200678·Kolbel type Glenoid Ret,2 prng 15mm, 300mm
POWDERED NATURAL RUBBER LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) 200 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE
FDA 510(k)
FDA Class 1
·General Hospital
ChoiceSpine Proliant® Posterior Pedicle Screw and Hook Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRASONIC IMAGING CATHETER - CORONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·April 24, 2014
COATED VICRYL PLUS ANTIBACTERIAL (POLYGLACTIN 910)
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·October 3, 2012
LIGAMAX-5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 27, 2010