11 results
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26ms
·
Sources: EU EUDAMED, US FDA
INFANT INCUBATOR, MODEL CHS-I1000
FDA 510(k)
FDA Class 2
·General Hospital
Sechrist Industries, Inc.
FDA UDI
SECHRIST INDUSTRIES, INC.·00852682007002·VENT,MILLENNIUM,ENGLISH,W/O S&P
BETELCARE SDN BHD
FDA registration
BETELCARE SDN BHD·1 product·🇲🇾 Malaysia
MEDICON YASARGIL CLIP APPLYING FORCEPS
FDA 510(k)
FDA Class 2
·Neurology
SUBDERMAL NEEDLE ELECTRODE FOR ELECTROENCEPHALOGRAPHY, MODELS PRO-E12SAF AND DEN-12SAF
FDA 510(k)
FDA Class 2
·Neurology
TESS GLENOID REVERSE HEAD DIAMETER 36
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016
PINN SECTOR HA ACET CUP 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 8, 2013
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 6, 2011
MEDFUSION 2010H SYRINGE INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code FRN·April 25, 2008
THE ELECTRODE STORE
FDA Adverse Event
Malfunction
·THE ELECTRODE STORE·Product code GXZ·July 17, 2021
The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018