23 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REPROCESSED COMPRESSION SLEEVES
FDA 510(k)
FDA Class 2
·Cardiovascular
Premier
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00856402006122·Decan Stopper Size 5 Closure 1/4
Bone Conductor B81
FDA UDI
PATH medical GmbH·04260223143113·Bone conductor for Sentiero
CASTENADA CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003903·CASTENADA CLAMP LARGE DOUBLE CURVED JAW ANGLED ...
CASTENADA CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921009090·CASTENADA CLAMP LARGE DOUBLE CURVED JAW ANGLED ...
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361005865·Arena-L, 35x26, Lordotic 8 degrees, 9H
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167100909220·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167100909260·
ALEUTIAN® Interbody Systems
FDA UDI
VB Spine LLC·10888857527911·AN Lordotic Spreader Size 8.5x28x4 mm, 12°
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167100909300·
NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ORAL/ENTERAL SYRINGES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
eXpress®
FDA UDI
NOVASTEP·03700879502304·Compressive staple 10-09-09
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·July 2, 2019
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013
9610617-2008-00010
FDA Adverse Event
Other
·Product code HRX·May 16, 2008
CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code KRH·May 24, 2011
NEOPUFF INFANT RESUSCITATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTL·January 15, 2017
ADULT INSPIRATORY-HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·February 20, 2012
RESPIRATORY HUMIDIFIER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 15, 2011