8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Hair Removal Device (Model: IPL-D26, IPL-D19)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD BBL™ CTA Medium™ with Sorbitol
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902216439·BD BBL™ CTA Medium™ with Sorbitol
ChoiceSpine Tiger Shark Cervical Spacer System
FDA 510(k)
FDA Class 2
·Orthopedic
HA ORBITAL IMPLANT
FDA 510(k)
FDA Class 2
·Ophthalmic
CAPTURE-R READY INDICATOR RED CELLS
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·March 25, 2011
FREEZOR XTRA 3
FDA Adverse Event
Malfunction
·CRYOCATH TECHNOLOGIES INC.·Product code OAD·October 26, 2008
ACCU-CHEK ® INFORM METER
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·August 24, 2011
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 1, 2013