8 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FLEX SCORING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Liner Inserter Suction Cap
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215018078·
EASY TOUCH
FDA 510(k)
FDA Class 2
·General Hospital
TRIAGE BNP TEST FOR BECKMAN COULTER IMMUNOASSAY SYSTEMS, MODEL 98200
FDA 510(k)
FDA Class 2
·Clinical Chemistry
INTERLOCK?-35
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KRD·October 8, 2014
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code LWP·June 8, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
ELEKTA LIMITED Precise Digital Accelerator, REF MRT 6001, MRT 6011; Medical Charged-Particle Radiation Therapy System Accelerator, Linear
FDA Enforcement
Class II
·Ongoing·Elekta, Inc.·December 13, 2023