7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Richard Wolf GmbH·04055207040768·PROCTOSCOPE TUBE Ø 18-24MM WL 113MM WL 113mm, ...
RAPID E
FDA 510(k)
FDA Class 1
·Microbiology
KFX PEEK BONE ANCHOR WITH PRE-ATTACHED SUTURES AND INSERTER HANDLE
FDA 510(k)
FDA Class 2
·Orthopedic
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES·Product code LZG·June 9, 2014
ADULT INSPIRATORY HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·October 26, 2010
UNICEL® DXC 660I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·December 21, 2012