8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
INTRA-AORTIC BALLOON PUMP MODEL KAAT
FDA 510(k)
FDA Class 2
·Cardiovascular
Arthrex®
FDA UDI
ARTHREX, INC.·00888867523944·Spine Compression Screw, 5.0x36mm
CHEMISTRY CONTROL N & A
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600
FDA 510(k)
FDA Unclassified
·Unknown
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 16, 2014
MX-PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV·Product code FPO·October 13, 2010
ALARIS
FDA Adverse Event
CAREFUSION 303, INC.·Product code FRN·November 12, 2012
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021