10 results
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18ms
·
Sources: EU EUDAMED, US FDA
Kepler II
FDA 510(k)
FDA Class 2
·Orthopedic
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575399673·Femoral stem prosthesis trial - Megasystem-C Tu...
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575399635·Femoral stem prosthesis trial - Megasystem-C Tu...
GENII GI 4000 ELECTROSUGICAL GENERATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NHANES WHOLE BODY DXA REFERENCE DATABASE
FDA 510(k)
FDA Class 2
·Radiology
STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 3
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·March 30, 2020
PINNACLE PELVIC FLOOR REPAIR KITS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 11, 2013
ASR ACETABULAR IMPLANT 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 8, 2011
IMMULITE 2500 STAT TROPONIN I
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·September 15, 2008
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 12, 2020